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Digging up the Bones

Microbiology
IMMUNOLOGY
Type I Hypersensitivity reaction

(anaphylactic and atopic)

Get reaction second time stung by bee; pre-existing IgE antibody specific for bee
venom is made on first sting.
Rash
Hives
IgE binds (Fe portion) to basophils and mast cells (Fe receptors).
Type II Hypersensitivity reaction -

(Cytotoxic)

IgM/IgG bind to cell antigen: lysis and phagocytosis. (i.e., Goodpastures)


Antibody can bind and lead to basement membrane damage.
Antibody can inappropriately excite TSH receptor.
Deposit complement on glomerular basement membrane.
Myasthenia Gravis, Immuno thrombocytopenia purpura, hemolytic
anemia, bullous pemphigoid and Graves disease. (NOT urticaria)
Type III Hypersensitivity reaction - (Immune Complexes)
Immune complexes lodge in a tissue and cause damage.
Antibody is complement activating antibody.
Ag-Ab complexes deposited
Hypersensitivity pneumonitis, Systemic Lupus Erythematosus (lip
swelling, skin rash, fever, inflammation of kidneys and joint pains),
Arthus reaction, Serum sickness
Type IV Hypersensitivity reaction -

(Cell-mediated, delayed type)

Delayed Type Hypersensitivity (DTH). CD4 is DTH T-cell MIF is a


mediator of DTH. Examples: Allergic contact dermatitis/TB skin test.
Part of normal immunity. After recognize antigen, T cells release
lymphokines and activate macrophages.
Paratope Epitope -

Antibody Combining site; the part of the antibody that binds to the
antigenic determinant.

Antigenic determinant.
(On a complex antigen.)
Bacterial DNA
May contain integrated sex plasmids and prophage

Peptidoglycan
Cell wall prevents rupture and gives shape.
Gram +, is thick but is susceptible to lysozyme.
Resistance to osmotic shock.
Gives rigidity of membrane.
Cell membrane
No sterols except mycobacterium
Bacteriophage That replicate their nucleic acid by means of a replicative
intermediate (or replicative form) would be expected to contain:
ssDNA
ssRNA
Repair of damaged bacterial DNA by photoreactivation (photolyase)
Does NOT require a DNA polymerase nor an excision of about 20
nucleotides adjacent to the lesion
Missense mutation - Would most likely be associated with a formation of a mutant
bacterial protein which is weakly functional (partially active)
DNA transcription and DNA replication
Both require Nucleoside triphosphates (not DNA polymerase III)
Microorganisms -

Can be both eukaryotic and prokaryotic

Sigma factor - Specificity for promotor site recognition resides with this factor of
bacterial RNA polymerase
Mutation in the deletion of 1 base pair in the middle of a structural gene coding for a
polypeptide
Results in changes in several amino acid residue within that polypeptide.
Establishment of the state of lysogeny requires functional host bacterial cell
ATP synthesis, ribosomes
Ouchterlony test
IgA
O
IgG

O O O IgM
AntiIgG

Infection of a sensitive bacterial culture with a temperate bacteriophage might result in:
Lysis of some of the cells

Lysogenic (phage) conversion of some of the cells


Transformation
In bacteria uptake naked DNA from solution into the cell.
Bacteria could acquire transposons
(No F factor needed)
Specialized transducing phage
Contains both phage and bacterial DNA
Can result in naturally formed recombinant DNA
Arises after aberrant excision of lysogen.
(NO sex factor needed)
Transduction
Requires a bacteriophage, (NOT a sex or fertility plasmid)
Requires bacterial virus
Co transduction
Map bacterial genes by random breakage of chromosome during phage
lytic growth.
Conjugation
Can result in passage of phage DNA from donor to recipient [F (fertility)
factor].
Bacterial conjugation and bacterial transduction
Differ in range of size of exogenetic DNA, (but dont differ in requirement
that the transferred genes be recombined by rec.-A mediated
recombination)
With bacteria that have abruptly acquired resistance to several antibiotics
the same resistance genes may be passed to recipient bacteria by these
ways.
Transduction passes transposons from bacterial cell to bacterial cell.
Transducing DNA
Found only in one cell within a colony arising following an abortive
transduction event
Transformation (NOT conjugation)
Bacterial gene transfer mechanism, used often to select recombinant DNA
molecules.
Lysogenization
Phage to prophage requiring ATP and ribosomes.
Example is diphtheria toxin.
Lysogenic (temperate) vs Lylic (virulent) bacteriophage
Different capacity to synthesize functional phage repressor protein.

Lytic bacteriophage replication requires host ATP and RNA polymerase.


dgal
Virus formed by aberrant excision of a prophage.
Hfr formation
Integrates F into the chromosome.
During bacterial conjugation, acts as a donor of chromosomal DNA.
Cannot transfer prokaryolic genes among bacteria by meiosis nor mitosis.
Phage chromosomes
Some contain only single-stranded RNA, some may be so small they have
genetic information sufficient for only 3 or 4 protein molecules.
Phage repressor protein
Ability to code for this is expected to differ in temperate and virulent
phage
Phage restriction endonuclease appears in:
Successful genetic recombination (after bacterial conjugation) was
observed to drop nearly 1000 fold following lysogenization of recipient
(F-) E. coli cells with P1 phage.
E. coli high frequency of recombination (Hfr) strain
Does NOT contain an extrachromosomal sex plasmid
Does NOT act as a recipient in bacterial conjugation
R factors in E. coli contain both:
Transposons and an element analogous to the sex (fertility) plasmid F.
Some plasmids
May not be able to initiate bacterial conjugation
May be carried within the head of a bacteriophage
Generalized transducing particles Contain bacterial genes (but not phage genes)
Antibody and macrophages (not cytotoxic T-lymphocytes, nor Natural Killer cells)
Most important in host defense against extracellular invaders
Mal Ser E. coli grows on : Glucose and 1 amino acid Serine media.
When separating lymphocytes on a density gradient
Lymphocytes are separated from red blood cells (not monocytes).
Red blood cells are more dense than lymphocytes

Immunoelectrophoresis -

Detects monoclonal gammopathy

RID -

Quantitative gel diffusion

Immunofluorescence -

Fluorescent labeled antibody binds to tissue antigen

ELISA -

Enzyme-Substrate reactions; measures the changes


in color, (NOT the radioisotope)
Not done in antigen excess.

Western Blot -

Definitive evidence for AIDS

RAST assay -

Measures specific antibodies against allergens, skin


test results.

The mouse
Class 1 MHC: H-2K and H-2D
A nude mouse has no thymus
The mouse MHC is called H-2
Syngeneic mice are genetically identical
HLA-D
Is called the immune response region in man.
It codes for antigens Important in cell-cell communication (Not code for
class I Ags)
Its antigens are present on -cells.
(does NOT code for certain complement proteins)
An assay for HLA-A, B, -C typing performed by cytotoxicity testing requiringAbs to known alleles to MHC
Trypan blue,
Complement,
(not cytotoxic T-lymphocytes)
May prevent Graft vs. Host disease which can result from bone marrow transplantation
Match MHC antigens of host and donor before transplantation
Pretreat bone marrow to remove mature T-lympocytes prior to
transplantation.
(Not remove all lymphoid cells and precursors from the marrow prior to
transplantation,
not use bone marrow from the mother for the transplantation)
Hyperacute graft rejection results when
Preformed antibodies prevent the graft from taking

Second set graft rejection is faster that First set rejection because:
Memory cells are present to facilitate a rapid response
MHC antigens are codominantly expressed every cell that expresses antigen expresses
both alleles.
T-cells see antigen in the context of MHC antigens.
CD2:

Receptor for Sheep Red Blood Cells (SRBC)


On majority of T-lymphocytes.
Is a monoclonal antibody that binds to SRBC receptor on thymocytes.
T11.

CD3:

T-cell receptor associated complex.

CD4:

Helper cell,
Small cortical thymocyte

CD8:

Suppressor cell,
Small cortical thymocyte

SRBC receptor:
CD2, T11, T cells. (NOT Fe receptor).
Valence -

Number of binding sites

Class -

Isotype

Suppressor T-cells
Regulate immune responses.
Express CD8+ (human) or Lyt 23+ (mouse) antigens.
Exert effects on helper T-cells, and B-cells to inhibit immune response.
CD3+, CD2+
(NOT activated by helper or inducer T-cells.)
Helper T-cells
CD4+
CD3+
CD2+
Lyt 1+23(-).
B-Lymphocytes
Triggered by:
Antigen binding to surface immunoglobulin,
Activated T helper cells.
Helper factors IL-1, IL-2, and BCGE.
Macrophages
Have a role in induction and amplification of immune response by:
Presenting antigen in an appropriate form to B and T-cells.

Expressing receptors for C3b, Fe part of IgG,m and lymphokines on their


membranes.
(NOT secreting lymphokines, and NOT by expression of antigen-specific
receptors on membranes.)
Macrophages and Neutrophils
Both have C3 receptors.
Both respond to chemotactic factors.
Both use lysosomal enzymes to kill bacteria.
Macrophages generate oxygen radical less efficiently than neutrophils.
(Both can NOT present antigens to T-cells).
Class I MHC
Cytotoxic T-lymphocyte (CTL).
Both B-cells and T-cells.
Class I antigens called Serologically Defined (SD).
Present on mast cells.
H-2K, and HLA-A.
Associated with beta2-microglobulin on surface.
T-Suppressor cells recognize antigens with MIIC class I molecules.
(Remember 1 x 8 = 8) CD8+
Class II MHC
(Remember 11 x 4 = 8) CD4+
Delayed type hypersensitivity T-cells (DTII)
Helper T-cell
Helper inducer
T-suppressor inducer cells
B-cells, macrophages and activated T-cells
Gene products are HLA-D
Lymphocyte Defined (LD)
Class II MHC genes:
Are expressed on B-cells
Are involved in cell-cell communication
Are called lymphocyte defined or LD genes
Are important in antigen presentation
C5a -

Most chemotactic molecule (not C5b, C3a, C3b, C1q)

C5a and LTB4 Spleen -

Directly chemotactic for neutrophils (NOT LPS, NOT 1L-2).


Neutrophils accumulate at inflammatory sites.

Contains antigen processing macrophages,


Is a secondary lymphoid organ
Is a site of antibody formation.

Opsonization Pathway to effective opsonization include:


Alternative complement pathway activation of C3.

IgG-antigen complexes alone (not IgM-Ag alone).


Classical pathway activation of C3.
Opsonins -

IgG1, IgG3, C3b, (NOT C8)

Congenital deficiency of the following complement components results in patient with


recurrent meningococcal infections
C8 and C5 (not C1-1NH, nor C2)
Activators of alternative complement pathway
Most bacteria,
Yeast cells,
Rabbi rbcs
E. Coli
Virus infected cells.
(NOT normal lymphocytes, NOT Sheep RBC)
Overall
Macrophages
release IL-1
excites T-cells
release IL-2
which increases Cytotoxic T-lymphocytes, Natural
killer cells, BCGF (B-cells growth factor), and T-cells.
Activation of classical pathway is more specific than alternate.
Antigen binding site
Binds to one epitope,
Has idiotypic determinants.
(NOT isotypic, NOT a hypervariable or constant regions.)
MHC complex
Involved in graft rejection
Cell communication
Host defense.
Anaphylatoxins C#a, C4a, and C5a (not C9a, Ba, C6a, C2a nor C1q)
Complement activators
Ag-IgG1 complexes
Ag-IgM complexes
Bacterial endotoxin
Fungal cell walls
(not neutrophil surfaces)
Participate in B-cell activation
BCGF,
Antigen, IL-2
Antigen-specific helper factors

IL-1:

Is produced by macrophages
Is a genetically unrestricted and an immunologically nonspecific factor,
Is a polypeptide cytokine and is stable at temperatures (-750C to +560C)
and pH (3 to 11).
Known as LAF (lymphocyte activating factor),
Excites T-cells for IL-2 production, reaction to injury and other purposes.
Induces differentiation of T-lymphocytes by increasing metabolism.
(Not only effects T-lymphocytes)
(NOT MHC restricted
NOT heat labile at high temp.)

IL-2:

Its major activity is it induces T-cell proliferation,


Excites CTLs
Excites BCGF, BCDF secretion and activates NK (natural killer) cells.
An immunologically non-specific T-cell growth factor.
Magnitude of T-cell clonal expansion depends on concentration of IL-2,
IL-2 receptor density, and affinity of receptor for IL-2.
(Unstimulated T-cells do NOT express IL-2 receptors.)
(does NOT act on its own secreting cell.)

Normal regulation of an immune response, the following events may occur to dampen
the response:
Induction of anti-idiotype antibodies
Production of high affinity IgG antibody to remove antigen from the
system.
Neutrophils have receptors for: IgG, C5a, and C3b (opsonins)
Metabolic stimulation of neutrophils includes:
H2O2 production,
Incr. Glycolysis,
Incr. Oxygen consumption.,
Decreased phagolysosomal pH
(Not incr.. enzyme synthesis)
TdT+:
Marker on pre-B and immature T-cells
Least mature T-cell.
Helper cells required for the activation of the following effector cells:
DTH and CTL (not macrophages and NK)
Suppressor cells are
CD8+
T8+
Ltl 23+
CD3+
Involved in regulation of B-cell response,
Regulate DTH and CTL responses
Decreased in patients with autoimmune disorders, but not absent.

Produce swelling (inject subcutaneously)


C3a, C2 kinin, C5a (NOT c3b)
Properdin
In alternate complement pathway, stabilized C3Bb.
The following could show an anamnestic response
B-cell
DTHT-cell
(not K-cell nor macrophage)
Specific immune response
To occur it is not necessary for T and B-cells to recognize determinants of
antigens.
CD4+:
Helper inducer,
Suppressor inducer,
Helper cells,
TDTH cells
In normal person, the number of CD4 lymphocytes is twice the number of
CD8 lymphocytes (ratio of 2:1)
(NOT suppressor effector, not TCTL)
(Not suppressor)
DTH (delayed type hypersensitivity) T-cell:
Is antigen specific
Releases lymphokines when activated
Response in positive skin test indicates a CMI response occurred
(NOT a helper cell for B-cell response.)
Mediators involved are: MIF, MAF,MCF and CD4+ cells (NOT CD8+
cells and NOT C-reactive protein.)
The effectors of protective cell-mediated immunity are
CTL (cytotoxic T-lymphocytes),
DTH (delayed type hypersensitivity T-cells),
(NOT neutrophils, nor B-cells)
Tc cells -

Do NOT recognize antigens with MHC class II molecules.

CTL -

Cytotoxic T-Lymphocytes
CD8+
CD3+
Lyt1-23+
CD2+

CMI against viral infection


Express CD8 and specific TcR/CD3 complex,
Recognize viral antigen with self MHC class I molecules.
TI antigens - (T-Independent)
Are often polyclonal B cell activators.
Excite B-cell to produce mainly IgM antibodies, and have
little or no anamnestic (secondary) response to second stimulation.
TD antigens (T-Dependent)
Can be IgE and IgA antibody-eliciting antigens.
Excite B-cells to make IgM antibody.
Generates anamnestic response to second stimulation (because antibody
switches to making IgG)
Antibody response, both T and B-cells have antigen specificity.
(Cell-cell contract is NOT essential).
A T-cell mediated Immune reaction can result in
Granuloma formation,
A DTH reaction,
Graft-versus-host disease,
Tumor cell destruction.
T-cell receptor complex
Recognized by anti-T3 (CD3) antibodies; the following cells express T3 antigens:
Cytotoxic T-lymphocytes,
Suppressor cells,
Helper cells
(not T-stem cells)
The effects of IL-2 on a precursor CTL that has not yet seen antigen in the context of
MHC:
NONE, since IL-2 receptors do not appear until after specific stimulation.
Altered-self means
The self-cell is altered (not the MHC antigens)
Myeloperoxidase deficient patients can still produce H2O2 O2, and O1I.
Marcophages
Present antigen to the helper T-cell.
Phagocytose and kill some pathogens.
Remove immune complexes from the circulation.
Release II,-12
Important host defense mechanism because:
Process antigen and present antigen with MHC Class II (1a) molecule.
Produce cytokines, and an immune response.
Have nonspecific effector functions for specific DTH (NOT CTL).

Have important role as APC (antigen presenting cell).


Survive after phagocytosis (Neutrophils do NOT).
Activated Macrophages
Have enhanced phagocytic activity.
Increased intracellular microbicidal activity.
Increased release of toxic produts (e.g., TNF).
Increased size and lysosomal content.
Macrophages
Are involved in:
Presenting antigen to B and T cells
Induration seen in DTH skin test,
(NOT involved in immediate wheel/flare skin test type I hypersensitivity)
Are the major cell type used as host cells by: amastigotes of cutaneous
leishmaniasis.
Adaptive immunity
Atopic allergy
Anamnestic response
Immunoglobulins
Specific antibodies,
DTH
(NOT interferons, NOT complement)
Innate Resistance
Comp;e,emt
Monocytes
Macrophages
Natural killer cells
C-reactive protein
(NOT natural antibodies, Not DTH)
Mature B-cell
When it can respond to immunogen by making antibody
IgD and other immunoglobulins (IgM), expressed on its surface
(Not when gene rearrangement of chain or express dId)
B-lymphocytesDevelopment begins in fetal liver,
Surface IgM, IgG, IgA
(NOT increased with MHC molecules nor IFN)
To determine if B-lymphocytes are functionally active the following tests should be
performed
Serum immunoglobulin levels.
Serum protein electrophoresis
(NOT natural killer cell assays

not mitogen assays with PHA)


To determine if T-lymphocytes are functionally active the following tests should be
performed
Skin test for delayed type hypersensitivity.
(NOT NK cell assay, nor assays for complement components, nor serum
immunoglobulin levels.)
The following systems of antigenic specificities would be useful in paternity testing
Allotypes
HLA antigens
Blood group antigens
(Not isotypes)
90% of the small cortical thymocytes
DIE
(so Not express T cell receptors, nor go to the Thymic medulla, nor go into
circulation.)
B cell primarily reside in
The primary follicles of the lymph node.
(NOT the cortex of the thymus, not deep cortical zones of the lymph node,
not follicles of red pulp of spleen.)
Antigen driven activation of B cells
Usually requires interaction of macrophages, B cells, T cells and antigen.
Leads to clonal expansion.
Occurs in the secondary lymphoid organs (NOT primary lymphoid
organs).
In the presence of antigen
A mature B cell can be activated
An immature B cell may become tolerant.
A pre B cell will NOT undergo gene rearrangements to form the
appropriate Ab.
A plasma cell will NOT be stimulated to divide.
B cell stimulated with DNP-BSA can cooperate with T-cell stimulated with ovalbumin
to produce an anti-DNP antibody response to DNP ovalbumin
In a 51Cr release assay, tumor cells release their 51Cr because they have been killed by a
cytolytic effector cell..
Lymphokines on the cells involved in an immune response
IL-1

IL-2

(gamma) IFN

Interferons
Are anti-viral substances
Augment NK activity, CTL and macrophage cytotoxicity.
IFN- is most species specific, and is heat and acid Labile lymphokine.
Are produced by leukocytes or fibroblasts
(Not susceptible to low or high dose tolerance, not induced by antiidiotype or anti-allotype antibodies.)
TNF

(Tumor nercrosis factor)


Macrophages - - - - - produce
Lymphocytes

TNF- = cachectin.
TNF- = Lymphotoxin/
Lymphokine

Excites IL-1 production from macrophages.


Excites fibroblast proliferation.
Primary lymphoid organs
Bone Marrow
Thymus
Secondary lymphoid organs
Spleen [B-cells mainly in white pulp / follicle (not medulla / red pulp)]
Lymph Nodes.
Thymus
Cortex is mostly immature lymphocytes, therefore cells with TdT and
CD1+
Monoclonal Antibodies: produced by fusing the following cells
Immune spleen cells and myeloma cells (HPGRT negative)
(Not normal spleen cells and myeloma cells (HGPRT positive)]
Cyclosporin A
Biological response modifier useful in heart, kidney, and bone marrow
Transplantation.
Inhibits T helper cell function.
Prevents IL-2 synthesis
Factors that influence tolerance induction
Low or high dose antigen (vs. optimum dose antigen).
Route of antigen administration.
(Not amount of IL-2 secreted nor expression of Class I molecules)
Preventing the activation of Immune responses to autoantigens, the following
mechanisms may occur
Clonal abortion,
Activation of specific suppressor T-lymphocytes.
(Not induction of IFN, nor production of T helper cells.)

BCDF -

(B-cell differentiating factor)


Is a lymphokine produced by T-cells,
Is a non-specific-MHC unrestricted lymphokine that induces proliferating
B cells to differentiate.
(Not a protein induced in macrophages by IL-1, not a glycoprotein on the
surface of B-cells)

Important in innate resistance


Macrophages,
NK cells,
Lysozyme,
CRP.
In Humoral immune response
The anamnestic Ab response requires CD4+ helper T cells
T-dependent (TD) antigen fails to stimulate antibody production in nude
mice.
T-independent (T1) antigen stimulates B cells to produce predominantly
IgM antibody.
TI antigen stimulates Ab production in nude mice
Host defense against mycobacterial infection is primarily due to
DTH response
(Not CTL, enhanced NK, nor Ab response)
Cytokines produced by T-DTH cells include:
(gamma) IFN,
MIF,
MCF,
(not TNF, NOT IL-1)
Have role in B-cell differentiation.
IL-4, IL-5, and IL-6.
TdT is present on
Pre-B and pre- T cells
(not on immature B cells, nor medullary thymocytes)
The idiotype of the surface immunoglobulin present on an early B-cell
Is reflected in the antigen binding site
Does NOT change when these cells are activated
Is the idiotype of secreted IgM
(changes NOT only when the DNA rearranges to allow isotype switching)
Tumor cell or virus infected target cell lysis by specific cytotoxic T lymphocytes
requires:
Cell-cell contact and specific recognition by T-cell receptor / T3
complex of CTL.
No antibody.

Divalent cations Mg 2+ and Ca2+ (Not complement)


Some antibodies against tumor target cells may block CTL killing of target cells, but may
help K cells to kill target.
Helper T-cells respond to:
IL-2,
IL-1,
Antigen in context of Ia,
(Not hapten)
NK cells
Are distinct from classical T and B cells.
Increased by IFN and IL-2
Are primarily LGL.
Are induced by tumor cells.
Have a degree of specificity more than macrophages but less than T. cells.
(do Not require natural antibodies to kill target cells.)
(NOT induced by natural antigens.)
(NOT restricted by class I or II molecules)
(Are NOT thymus derived cells.)
IFN -

(Interferon)
Increase NK activity, therefore used in immunotherapies,
Have anti-proliferation activity against tumor cells,
Immunoregulatory activities.
(NOT lymphokines)

Cytotoxic lymphocytes (CTL)


Recognize class I MHC
Have surface markers: CD2, CD3, and CD8 (not CD4)
ADCC -

Mediated by:
K cells (by expressing receptors for the Fe portions of IgG)
NK cells,
Macrophages.
(NOT B-cells)

Avidity -

Measure how strong a polyclonal or monoclonal antibody binds to a


complex antigen.
Measures strength of binding, equal to the same determinant of different
complex negatives
Probably weaker to cross-reactive epitope or avidity.

Affinity

Codominant expression
Products of both alleles are expressed on all positive cells.
Magnitude of T-cell clonal expansion is dependent upon

IL-2 concentration,
IL-2 receptor density,
The duration of IL-2, IL-2 receptor interaction,
Affinity of the receptor for IL-2.
Cyclosporin A
Inhibits helper T-cells.
Prevents IL-2 synthesis
(Not a potent suppressor T-cell activator, not inhibit B-cells)
Non-immune early response to viral infections involve:
Interferons,
Natural killer cells,
Complement,
(Not cytotoxic T-lymphocytes)
Hybridoma technology produces Monoclonal antibodies which
Can cross react with tow different antigens
Can be made without having a pure antigen.
Important as a research tool, and has application for clinical medicine,
(Not Increased specificity following absorption with cross-reacting
antigens).
Western Blot
Used to confirm HIV antibodies.
Known HIV antigens separated using electrophoresis.
Goal is to confirm a positive ELISA.
Positive bands when antibodies from patient serum binds to HIV antigens.
T cell Receptors
Both alpha and beta chains, have variable and constant domains.
Recognize antigen in the context of MHC class I or classes II.
(MHC Class II or la antigen do NOT fix complement)
(CTL doesnt recognize and kill specific virus-infection target cells
because CTL recognize mainly virus antigens in the context of MHC class
II antigen.)
It is easier to induce tolerance in neonates than adults.
Felton demonstrated dose dependent tolerance.
If mother had measles or measles vaccination, her baby may not respond well to the
measles vaccine before 12 months of age.
Suppress and immune reaction by
Antigen specific suppressor cells
Nonspecific suppressor cells,
Monocytes,
B-cell products.

B cell tolerance
May occur if a single signal is received by a B cell
Is easier to induce in immature B-cells than mature B-cells
May be mediated by anti-idiotypic Ab.
May be either low zone or high zone or high zone tolerance.
Severe combined immunodeficiency
(Not complement/B/T-cell immunodefic.)
is suggested by the combination of overwhelming and repeated viral,
fungal, Hemophilus and Streptococcus infections.

Suppress and immune reaction by Antigen specific suppressor cells,


Nonspecific suppressor cells,
Monocytes,
B-cell products.
B cell toleranceMay occur if a single signal is received by a B cell.
is easier to induce in immature B-cells than mature B cells.
May be mediated by anti-idlotypic Ab.
May be either low zone or high zone tolerance.
Severe combined immunodeficiency(Not complement/B/T-cell immunodefic.)
Is suggested by the combination of overwhelming and repealed viral, fungal,
Hemophilus and Streptococcus infections.
AIDS patients areInfected with HIV-1, HIV-2, or LAV.
Infected with, HTLV-III.
Infected with CD4+ T cell trophic retroviruses.
Infect CD4+ cells, destroy T-helper cells, and decrease CMI.
See polyclonal B cell activation / hypergammaglobulinemia.
See depressed lymphocyte count (not normal levels) with reversed T4/T8
ratio.
Lymphopenia.
NOT primary immunodeficiency disease, it IS a secondary
Immunodeficiency disease.

May die of pneumocystis carinii, or CMV infection.


Virus could infect T helper cells, monocytes, macrophages, glial cells and
any CD4+ cells.

(NOT Infected with IITLV-II retroviruses, not increase in NK cell activity)


Immunodeficiency Result of Malignancy and aging.
(NOT from vaccination and Increased intellectual activity.)
Immunodominant
The most immunogenic determinant of a complex antigen.
Second set Graft rejection involves:
CMI.
CTL,
DTI IT-cells.
(NOT antibody)
Antibody role In regulation of Immune response:
Feedback inhibition of immune response caused by high affinity IgG

antibodies Interfering with antigen presentation.


Idiotype-anti-idiotype network.
Affects immunogenicity of antigen by complexing with antigen.
(Does NOT provide specific antibody to arm suppressor T cel Is.)
Immunize goat with rabbit bodiesWill produce anti- isotype antibodies.
Treat the following by Passive ImmunizationB-cell immunodeficiency (NOTT-cell ID).
Rabies.
(NOT autoimmunity)
A Mixed Lymphocyte Response (MLR)Measures I ILA-D differences.
Lymphocytes are dividing in response to IILA-D allele (NOT A, B, or C).
mostly B cells, MHC class II (Ia antigens).
(NOT measures 311-thymidine release,
not called a plaque assay
not used to characterize Class I MI IC Alleles)
Light chain genesdo Not have D, diversity region gene segments
but do have:
V, variable region gene segments.
J, Joining region gene segments.
C, constant region gene segments.
Ig classes can be distinguished based on their HEAVY chains (NOT light chains).
With regard to molecular weight IgG is larger than kappa chains.
IgM is larger that IgG.
Secretory IgA is usually larger than serum IgA.
(Feb fragments are NOT larger than IgG.)
General topography of an immunoglobulin gene has-Leader sequences, Intron sequences,
Exon sequences.
In Serum Electrophoresis, y-globulins have:
The negative charge of the 5 protein fractions,
A net mobility to the anode.

IgG:

The primary effector functions of IgG are:


Opsonization
(Not Incr. vasodilation, not binding to basophils)
The IgG gene, is composed of:
One exon for each constant domain.
A hinge region exon.
DNA.
IgG crosses the placenta,
At birth serum IgG is > IgM.
When human IgG is injected into a rabbit, isotypic specificities antibodies
are the predominant antibodies.
The concentration of normal adult serum IgG is approximately 10 mg/ml.
(or 1000 mg/dl)
The number of subclasses of human IgG is:
4 (four)
When IgG is digested with pepsin the following fragments are generated:
F(ab)2 which have two antigen binding si sites fragment. (Fragments will f ix
complement.)

IgG molecule:
The light and heavy chains are identical.
The carbohydrate is in the constant region of heavy chains.
(The hinge region does not join heavy and light chains.)
The IgG and the fragments of IgG were isolated from anti.- sheep red
blood cell antiserum: Agglutination occurs if IgG and sheep red blood cells
F(ab)2 and sheep red blood cells
(not Fab and sheep rbc, not Fc and sheep rbc)
In a secondary antibody response IgG >IgM.
IgA:

Is the predominant immunoglobulin class in secretions.


Has one J chain.
Two subclasses of human IgA.
Secretory IgA has both SC (secretory component) and J chain.
Secretory IgA present in tears, but NOT present in serum.
Does NOT cross the placenta.
(Does Not fix complement by the classical pathway,
does not bind to phagocytes)
Protects against human shigellosis,
Found in saliva.

IgM-

A pentamer.
Immunoglobulin class with greatest molecular weight.
Is Initially produced by most B cells.
(NOT produced by switching from IgA.
not encoded by 12 centimorgans 5 of the centromere of chromosome 4)
Serum IgM:
Has J chain
Is a pentamer
(Does NOT have 2 Ab combining sites per molecule,
Not fix complement less efficiently than igG)

IgE-

Involved in type I hypersensitivity,


Binds firmly to mast cells and triggers anaphylaxis,
Plasma cells produce immunoglobulins.

Highest concentration of antigen X is found with lowest cpm.


Highest concentration of radial diffusion assay is seen with highest diameter.
Highest titer in a hemagglutination assay in Inst agglutinated tube: (spread out not dot)
Serum IgM and membrane IgM have different properties for the followingSize of heavy chain,
Molecular weight,
Number of I chains.
(Not size of light chains)
Idiotypic determinants.
Can induce anti.-idiotype Abs.
Are found in variable regions.
(Not found In constant . )
(can NOT produce anti.-allotype Abs)
Isotypic determinantsIdentify classes.
Are found on constant regions.
Are present among gamma globulins.
(NOT found on variable regions)
The product of one normal plasma cell
Has two identical light chains and two identical heavy chains.
Kappa and Lambda light chainsAre encoded on chr. 2 and 22 in man.
(NOT same chromosome, do not each have multiple constant regions)

Secretory component is found in secretory IgA (not serum IgA only, not secretory IgG,
not IgE)
In most organ specific autoimmune diseases there is a strong association between the
disease an d HLA allele.
Immune responseImmunogen injected in the muscle > Immunogen taken orally.
If immunogen given to a 25 yr. old > If administered to a 10 year old.
Foreign immunogen > self immunogen.
Particulate immunogen > soluble immunogen
In rheumatic fever, the possible mechanism for inducing the autoimmune phenomenon isInfection with Streptococcus group A, a bacteria similar to host antigen.
To prove by Witebskys postulates that Juvenile Diabetes is an autoimmune disease,
Antibodies to the pancreas must beFound in most affected individuals.
Capable of causing the destruction of the pancreas when injected into
another member of the animal model.
(Not capable of Inducing anti-idiotype Abs when injected into an animal not
able to Interact with MIHC molecules)
Brutons agammaglobulinemia X-Unked.
Pyogenic bacterial infections.
Pt. has recurrent infections with extracellular organisms.
Pt. has IgG levels less than 0.5 mg/ ml (50 mg/dl).
(not usually female, not unusually high T-suppressor cell counts.)
(NOT intracellular, not infections from viruses)
DiGeorge Syndrome- pt. has...
Failure to produce IgG In response to T-dependent antigens, causes a
Decrease in the number of helper T cells.
Little or no thymic tissue.
Few lymphocytes (<1500/cu mm). Decreased or absent T-lymphocytes.
Depressed or no IL-2 production.
(Not extremely high IgG levels,
NOT failure of bone marrow to develop normal,
NOT secondary immunodeficiency,
B-Cell lymphomaCell has DNA rearrangement detected by Southern blot using an
immunoglobulin DNA probe.
T-Cell lymphoma
Cell has DNA rearrangement detected by Southern blot using T-cell DNA
probe.

Macrophage cell line


Cell has NO rearranged DNA detected by either probe.
Autoimmune disease
Systemic lupus erytematosusEncephalomyelitisHashimotos diseaseMyasthenia gravisJuvenile Diabetes-

Target antigen
DNA
Neural tissue
Thyroid
Acetylcholine receptor
Pancreas

DO NOT Suspect a primary immunodeficiency for a 65 yr. old with recurrent infections,
total immunoglobulin levels are 35 mg/mi with a monoclonal spike by serum protein
electrophoresis.
Rh(-) woman is pregnant with her first Rh+ childIf fetal blood enters her circulation it will initiate a primary immune
response.
IgM and IgG antibodies will be produced in response to Rh antigens. Second
Rh+ child may have erythroblastosis fetalis if she did not prevent
immunization against Rh of first child with passive immunization.
(NOT since she is Rh- she has preformed anti-bodies to Rh antigens,
not Ab to Rh antigens is exclusively IgG)
Antibodies against Rh isoantigens cause erythroblastosis fetalis
Since can bind to and agglutinate rbcs of an Rh baby.
Since they are IgG antibodies and can cross placenta
(NOT IgM)
.
Type B blood
ABO blood typing, serum will agglutinate blood from a type A
individual
Has anti-A antibodies in serum.
Rbcs will agglutinate in the presence of an equivalent concentration of
anti-B antiserum. (Agglutinates with anti-B antibodies.)
NEGATIVE agglutination will look like a button of rbcs on the bottom of the
tube.
(Serum does not have anti-B anti bodies in it.)
Type AB bloodHas NO antibodies to ABO blood.
Will agglutinate if incubated with anti-A or anti-fl antiserum, since it has
both A and B antigens.
Hapten- Can be immunogenic if attached to a carrier molecule,

Small
DNP
Epitope and an antigen (but N01 an immunogen/ mitogen)
(Not LPS)
Monoclonal Antibody binds to 2 complex antigens with different avidities
This could result from the antibody binding to similar determinants on the
2 antigens.
The same determinant could be present In different concentrations on the
2 antigens.
This is possible.
(Not result from the monoclonal Ab binding to 2 completely different
determinants on the antigens.)
Need an antibody with a valence of 2 or more for
Agglutination
Precipitation
Hemagglutination
Lattice formation
The following cells can respond to specific AntigenActivated 0 cell
(NOT cortical thymocyte, plasma cell, nor Ia positive macrophage)
Anti-mumps titer of serum from A Is 1,520 and the anti-mumps titer of serum front B I:
2; the following are possible individual A has had mum~.
Individual A has been vaccinated against mumps.
Individual B has not been exposed to mumps.
Individual B has not been vaccinated against mumps.
In Laboratory, in the Pregnancy assayUrine was tested for the presence of Human Chorionic Gonadotropin
(HcG).
If no HcG was present In the urine, anti-HcG would agglutinate HcG
coated latex particles.
If HcG was present in urine, reactivity of antibody was removed.
Results can be obtained In a matter of a few minutes.
Positive if NO agglutination, because urine HcG neutralized the anti-HcG.

Lines of identity in an Ouchterlony


Indicate that two antigens are similar with respect to the specificity of the
antibody in the opposing well.
(Not appear in areas of antibody excess,
not develop within 2 hours,
not indicate that 2 antigens are identical)
Determine presence of same protein in sera from 2 different sources.
Trypan blue exclusionAssay used for tissue typing (I ILA-A, B, and C) by utilizing complement
mediated lysis (stains dead cells), requires typing antisera against appropriate
alleles.
Used clinically.
(does NOT measure cell division, NOT a difficult lest.)
C5a:

An anaphylatoxin (also, C3a and C4a)


Chemotactic
(NOT neutralize viruses,
NOT an opsonin)

C3b:

In both alternative and classical pathways of complement activation can


react with other serum components to form an enzyme which cleaves C3.
It is an opsonin.
(NOT an anaphylatoxin,
does NOT react directly with iron)

T-cells-

Thymus: Stem cells ---> T-cells,


Function in cell-mediated immunity,
Have membrane antigenic determinants different from B cells,
Important in IgA antibody response.

B LymphocytesHave an integral membrane Ig on their surface.


Major histocompatibility class I antigensPolymorphic surface proteins on virtually all cells.
MHC Class I Wide cell distribution, Contains beta 2 microglobulin
Composed of 2 non-covalently linked polypeptide chains (Not of equal
molecular weight), present on most cells and almost all nucleated cells
(Not just B lymphocytes).
HLA-A, HLA-B, HLA-C (Not T1a).
The A locus encodes for Class I antigens, serologically defined by
microcytotoxicity testing.
CD8 + cytotoxic T-lymphocytes recognized antigen of MIHC I recognized by
CTL effectors.

MHC Class II Antigens

Composed of 2 non covalently linked polypeptide chains ( and ).


CD4 + helper T-lymphocytes recognize antigen as MHC II.
On surface of antigen-presenting cells that activate helper T cells.
F(ab)2 fragmentsResult from cleavage of IgG by pepsin,
Have 2 combining sites for antigen.
Fab fragment and N-terminal amino acids

Fixes complement
Antigen interacts with IgE - (atopy)
Causes hay fever and Prausnitz-Kustner reaction.
IL-1:
Fever,
NOT pain.
PGE2:

Pain

LTD4:

Neutrophil activation

Neutralizing antibodiesLargely responsible for preventing influenza virus infection.


Terminally-differentiated B-lymphocyte = an antibody secreting plasma cell.
Amplification of host defense reactions By activating coagulation, fibrinolytic, and bradykinin-generating paths.
cause: leukocyte recruitment, vasodilation, and increased capillary
permeability, neutrophil margination and trans-endothelial migration
Abortive bacterial transductionDNA fragments fail to replicate within recipient cells.
Type III hypersensitivityAntigen-antibody complexes deposit in tissue, complement binds, and
inflammatory events lead to tissue damage.
Recipient with HLA Antigens
HLA-A I, HLA-B, DW1, DW5 lymphocytes to stimulate a minimal mixed
lymphocyte response (MLR) with this patient must have DW1 and DW5

Antigenic drift
Many times involves single nucleotide base change in a virus genome.
Contributes to minor antigenic changes in hemagglutinin, and
Neuraminidase of influenza viruses.
T cell maturation
Rearrangement of DNA which codes for T-cell receptor.
Migration to cortex to the medulla
Migration to periphery.
Division in response to stimulating antigens.
Anamnestic response is faster and more specific, longer lasting and greater then primary
immune response.
Infection -

Of a sensitive bacterial culture with a bacteriophage result in:


Lysogeny,
Vegetative phage reproduction (lytic cycle),
Integration of phage nucleic acid within bacterial chromosome,
Lysogenic conversion.

Primary lymphoid organ = bone marrow


Secondary lymphoid organ = Spleen

BACTERIOLOGY
Gram Positive bacteria
Have teichoic acids,
Have muramic acid
Have greater peptidoglycan than gram negative bacteria
Can convert to protoplasts
Gram Negative bacteria
Have peptidoglycan,
Have muramic acid,
Have flagella, O-antigens, pili, mesosomes,
Have endotoxin with outer membranes
(do NOT have endospore)
Staphylococcus aureus
Gram + cocci,
Produces coagulase,
Catalase positive
Mannitol fermentation
Perform a catalase test, the an accustaph test
Certain strain produces an exfoliative toxin and a disease called Scaled Skin
Syndrome
Outbreak of Staph food poisoning from contaminated common food supply.
Strep. Pneumonia Gram + cocci, alpha-hemolytic, bile+, Optochin + (zone of inhibition)
Cryptococcosis -

Differential diagnosis should include TB

Cryptococcus neoformans
(Not acid-fat,
Not cause chronic subacute mycosis
Not cause mycetoma, dermatomycosis, not griseofulvin D.O.C.)
Rheumatic Fever -

Latex Agglutination TestsIndia ink test-

Immune response to strep. pyogenes group A.


Increase ASO titer, diagnosis.
Penicillin = D.O.C., long-term, cardiac
Identify:
Staph aureus
Strep. pyogenes group A
Positively identifies Cryptococcus neoformans
If stool sample for anaerobes Clostridium difficile

Prions

Diseases are confined to CNS,


have prolonged incubation periods,
have progressive course leading to death
(Are NOT exclusively in humans)

Lipopolysaccharide = an Endotoxin
Endotoxin -

Lipid A
Causes gram (-) sepsis
Fever and endotoxic shock
Hypotension and anoxia of organs like heart, lung and brain

Dipicolinic acid is found in bacterial endospores.


Composition of cell wall determines whether a bacterial cell stains gram + or (-)
M protein; there are 62 types group A strep
Disease: Granuloma inguinale
lesion.

Donovan bodies are seen from histology of genital

Bacterial division lacks mitotic process.


Bacteroides
Gram negative rods in anaerobic disease
SOD (superoxide dismutase)
In aerobic bacteria
(NOT in anaerobic bacteria)
SOD ( superoxide dismutase) and catalase
Allows facultative bacteria to be tolerant to superoxide and H2O2.
Obligate anaerobe bacterial pathogen
Usually lack SOD and / or catalase.
Core polysaccharide
Made of 5 sugars: Glucose, galactose, N-acetylglucosamine, heptose, and
keto-deoxyo oclulonic acid.

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