90) The EBV antigen fragments will be presented by the virus-infected cells along with
A) complement.
B) antibodies.
C) class I MHC molecules.
D) class II MHC molecules.
E) dendritic cells.
Use the following information as background for the next few questions.
Immunodeficiencies can be genetic in origin, and two examples are Bruton’s agammaglobulinemia, an
X-linked disorder, and DiGeorge syndrome, caused by a deletion from chromosome 22. Bruton’s
disorder results in underdeveloped B cells, whereas DiGeorge syndrome results in a missing or seriously
underdeveloped thymus.
91) Select the description that likely indicates a child with Bruton’s disease.
A) baby girl Denise, with low level of antibody response to streptococcal infection
B) baby boy John, with immature T cells, missing CD4 receptors
C) baby boy Jeff, with no plasma cells following infection by bacterial pneumonia
D) baby girl Susan, with no evidence of a thymus gland
E) baby boy Matt, with very low circulating antigens
92) Bruton’s disorder will likely include
A) the failure of heavy-chain gene rearrangement in B cells.
B) the failure to incorporate CD4 receptors into cell membranes.
C) an underexpression of the gene for the β chain of the T cell receptor.
D) an underexpression of the gene for the CD8 receptor molecule.
E) the inability of the bone marrow cells to interact with MHC molecules.
93) Assume that a DGS-like phenotype was produced in a specific “gene-knockout” mouse, one lacking
expression of HA3, a Hox gene known to be involved in developmental regulation in the mouse.
The phenotype of the HA3 knockout can be ascertained by
A) a bone marrow biopsy.
B) an assay for environmental agents known to cause birth defects.
C) a chest X-ray.
D) the measurement of the proportion of CD4 cells to total lymphocytes.
E) an autopsy examination of the adrenal glands.