MHC Flashcards
Exogenous antigen includes all of the following EXCEPT
a. bacterial toxins.
b. extracellular protozoan parasites.
c. most bacteria.
d. ragweed pollen.
e. viruses.
e. viruses.
Human Class I MHC a chain molecules are
a. b2-microglobulin.
b. H-2 D, K, and L.
c. H-2 IA and IE
d. HLA-A. -B, and -C.
e. HLA-DR, -DP, and -DQ.
d. HLA-A. -B, and -C.
Cells which have MHC Class II are ________, which present ________antigen to Th cells.
a. antigen presenting cells, endogenous
b. antigen presenting cells, exogenous
c. infected cells, inflammatory
d. target cells, endogenous
e. target cells, exogenous
b. antigen presenting cells, exogenous
Signaling to a cytotoxic T cell that a liver cell is infected with hepatitis virus depends on
a. binding of Ii to Class I MHC until the peptide is loaded.
b. binding of TCR on the cytotoxic T cell to Class II MHC on the infected cell.
c. binding of processed antigen to liver cell Class I MHC.
d. processing the hepatitis virus peptides to the correct size and anchor residues in the endosomal pathway.
e. both c and d are correct.
c. binding of processed antigen to liver cell Class I MHC.
Endogenous antigen presentation requires delivery of antigen peptides to the endoplasmic reticulum by
a. Class I MHC and invariant chain.
b. calnexin and tapasin.
c. HLA-DM.
d. leader sequence.
e. TAP-1 and TAP-2.
e. TAP-1 and TAP-2.
Following virus infection, peptides produced from the proteasome are more likely to be presented on the surface of the target cell because
a. MHC Class I is synthesized in response to virus infection.
b. proteasomal enzymes which produce shorter peptides are synthesized in response to virus infection.
c. TAP-1 and TAP-2 specifically bind virus peptides.
d. virus amino and carboxyl terminal amino acids bind better to Class I MHC than peptides from self proteins.
e. virus infection induces expression of proteases which cut proteins at sites which bind best to TAP-1 and TAP-2.
e. virus infection induces expression of proteases which cut proteins at sites which bind best to TAP-1 and TAP-2.
Exogenous antigen is processed
a. after presentation by antigen presenting cells.
b. by nearly every nucleated cell.
c. by the cytosolic processing pathway.
d. in the presence of b2-microglobulin.
e. in acidified endosomes.
e. in acidified endosomes.
Class II MHC does not efficiently present endogenous antigen because
a. antigen synthesized inside the cell never makes it to the endosomal compartment.
b. endogenous antigen cannot be processed into peptides small enough.
c. HLA DM transports Class II to the surface before it can bind endogenous peptide.
d. invariant chain blocks binding of endogenous peptide in the ER.
e. phagocytosed antigen binds Class II as rapidly as Class II is synthesized.
d. invariant chain blocks binding of endogenous peptide in the ER.
MIIC is a specialized intracellular compartment where
a. HLA DM promotes the release of CLIP and peptide binding to Class II MHC.
b. invariant chain binds to Class II MHC a and b chains.
c. peptides are transported into the ER for binding to Class II.
d. proteins are broken down into peptides by proteasomes.
e. some pathogens live protected from lysosomal enzymes.
a. HLA DM promotes the release of CLIP and peptide binding to Class II MHC.
In order to have pathogen peptide plus Class II MHC molecules expressed on the membrane of host cells, all of the following are required EXCEPT
a. b2-microglobulin.
b. CLIP.
c. HLA-DM.
d. HLA-DR, -DP, and -DQ alpha chains.
e. Ii .
a. b2-microglobulin.
Invariant chain (Ii)
a. inhibits binding of endogenous peptide to Class I MHC.
b. is degraded in the MIIC compartment to CLIP.
c. is released from Class II upon binding of b2-microglobulin.
d. is the constant region of Class I peptide binding site.
e. prevents exogenous peptide binding to Class II MHC in the ER.
b. is degraded in the MIIC compartment to CLIP.
Antigen binding by Class I MHC molecules
a. accommodates many different peptides.
b. preferentially occurs for peptides 13-18 amino acids in length.
c. occurs at a site on Class I MHC formed by folding of a1 and b2-microglobulin domains.
d. occurs only on antigen presenting cells.
e. takes place at the plasma membrane of the infected cell.
a. accommodates many different peptides.
Both Class I and Class II MHC molecules are
a. composed of a and b chains with variable and constant regions.
b. expressed constitutively on all nucleated cells.
c. expressed on the B cell membrane.
d. part of the T cell receptor for antigen.
e. synthesized in response to antigen processing.
c. expressed on the B cell membrane.
The major histocompatibility complex has
a. dozens of loci for Class I and Class II proteins.
b. genes that encode proteins associated with antigen processing.
c. only genes encoding Class I and Class II molecules.
d. single loci for Class I and Class II proteins.
e. three regions encoding Class I, Class II, and Class III receptors.
b. genes that encode proteins associated with antigen processing.
MHC polymorphism
a. is generated by recombination of HLA A, B, and C gene segments.
b. is present primarily in the peptide-binding regions of MHC proteins.
c. is the result of random association of many alpha and beta genes.
d. restricts the ability of B cells to bind antigen.
e. results in expression of dozens of MHC alleles on each APC.
b. is present primarily in the peptide-binding regions of MHC proteins.