Small molecules that must combine with large proteins to become immunogenic are called:
a. Complete antigens
b. Kinins
c. Antigenic determinants
d. Haptens
Small molecules that must combine with large proteins to become immunogenic are called:
a. Complete antigens
b. Kinins
c. Antigenic determinants
d. Haptens
Which of the following cell types are antigen-presenting cells (APCs).
1. Macrophages 2. Neutrophils 3. B cells 4. T cells 5.Plasma Cells
Mark the following statements as true or false. If a statement is false, correct is to make a true statement.
The secondary immune response is mediated by plasma cells.
How does a cytotoxic T cell destroy another cell displaying antigens bound to class I MHC proteins?
Although the adaptive immune system has two arms, it has been said, 'no T cells, no immunity.' Explain.
Mr. White developed neutropenia as a consequence of cancer chemotherapy, which destroyed much of his bone marrow. What other components of the immune system would be harmed by bone marrow destruction? Would you expect his hematocrit to be elevated or decreased? What effects would you expect to see from this change in hematocrit?
Mr. James, an 80-year-old man, is grumbling about having to receive a flu shot every year. Flu viruses have a high mutation rate (undergo rapid genetic changes), which results in the appearance of new proteins on the flu virus's 'coat.' How does this help explain the need to get a flu shot each year?
Blocking the antigen receptors on the surface of lymphocytes would interfere with
(a) Phagocytosis of the antigen
(b) That lymphocyte's ability to produce antibodies
(c) Antigen recognition
(d) The ability of the lymphocyte to present antigen
(e) Opsonization of the antigen
Differentiate between humoral and cellular adaptive immunity.
Mark the following statements as true or false. If a statement is false, correct it to make a true statement.
The immune response to a viral infection involves NK cells and different kinds of lymphocytes.
CD4 markers are associated with
(a) Cytotoxic T cells
(b) Regulatory T cells
(c) Helper T cells
(d) All of these