BOC Study Guide PART 2 (CHAPTER REVIEW) Flashcards
(134 cards)
- Which of the following is a true statement about Bruton
agammaglobulinemia?
a. it is found only in females
b. there are normal numbers of circulating B cells
c. there are decreased to absent concentrations of immunoglobulins
d. the disease presents with pyogenic infections 1wek after
birth
c. there are decreased to absent concentrations of
immunoglobulins
- Immunodeficiency with thrombocytopenia and eczema is often
referred to as:
a. DiGeorge syndrome
b. Bruton agammaglobulinemia
c. ataxia telangiectasia
d. Wiskott-Aldrich syndrome
d. Wiskott-Aldrich syndrome
- Which of the following has been associated with patients who have homozygous C3 deficiency?
a. undetectable hemolytic complement activity in the serum
b. systemic lupus erythematosus
c. no detectable disease
d. a lifelong history of life-threatening infections
d. a lifelong history of life-threatening infections
- Hereditary deficiency of early complement components (C1, C4
and C2) is associated with:
a. pneumococcal septicemia
b. small bowel obstruction
c. lupus erythematosus like syndrome
d. gonococcemia
c. lupus erythematosus like syndrome
- Hereditary deficiency of late complement components (C5, C6,
C7 or C8) can be associated with which of the following conditions?
a. pneumococcal septicemia
b. small bowel obstruction
c. systemic lupus erythematosus
d. a systemic Neisseria infection if exposed
d. a systemic Neisseria infection if exposed
- Combined immunodeficiency disease with loss of muscle coordination is referred to as:
a. DiGeorge syndrome
b. Bruton agammaglobulinemia
c. ataxia telangiectasia
d. Wiskott-Aldrich syndrome
c. ataxia telangiectasia
- A patient with a B-cell deficiency will most likely exhibit:
a. decreased phagocytosis
b. increased bacterial infections
c. decreased complement levels
d. increased complement levels
b. increased bacterial infections
- A marked decrease in the CD4 lymphocytes and decrease in the
CD4/CD ratio:
a. is diagnostic for bacterial septicemia
b. may be seen in most hereditary immunodeficiency disorders
c. is associated with a viral induced immunodeficiency
d. is only seen in patients with advanced disseminated cancer
c. is associated with a viral induced immunodeficiency
- A patient underwent renal transplant, receiving a kidney from an
unrelated donor. This type of transplant is termed:
a. allograft
b. syngraft
c. autograph
d. xenograft
a. allograft
- Which of the following is a hyperacute reaction that is not part of
chronic cell-mediated transplant rejection?
a. narrowing and occlusion of graft blood vessels
b. reaction of T and B cells to graft antigen
c. antibodies to MHC antigens on white cells
d. arteriosclerosis of the graft arterial wall
c. antibodies to MHC antigens on white cells
- Incompatibility by which of the following procedures is an absolute
contraindication to allotransplantation?
a. MLC (mixed lymphocyte culture)
b. HLA typing
c. Rh typing
d. ABO grouping
d. ABO grouping
- Graft-versus-host disease is:
a. initiated by the recipient
b. a minor concern in bone marrow transplant
c. asymptomatic in most cases
d. initiated by the donor
d. initiated by the donor
- Bone marrow transplant donors and their recipients should be preferentially matched for which antigen system(s)?
a. ABO-Rh
b. HLA
c. CD4/CD8
d. Pla1
b. HLA
- A 28-year-old man is seen by a physician because of several months of intermittent low back pain. The patient’s symptoms are suggestive of ankylosing spondylitis. Which of the following laboratory studies would support this diagnosis?
a. a decreased synovial fluid CH50 level
b. low serum CH50 level
c. positive HLA-B27 antigen test
d. rheumatoid factor in the synovial fluid
c. positive HLA-B27 antigen test
- HLA-B8 antigen has been associated with an increased incidence
of which of the following pairs of diseases?
a. ankylosing spondylitis and myasthenia gravis
b. celiac disease and ankylosing spondylitis
c. myasthenia gravis and celiac disease
d. Reiter disease and multiple sclerosis
c. myasthenia gravis and celiac disease
- HLA typing of a family yields the results in this table:
On the basis of these genotypes, predict the possibility of ankylosing spondylitis in this percentage of their children.
a. 25% of their children
b. 50% of their children
c. 75% of their children
d. 100% of their children
b. 50% of their children
- Alpha-fetoprotein, an oncofetal antigen, is least likely to be found
in:
a. pregnancy
b. hepatocellular carcinoma
c. cirrhosis
d. breast carcinoma
d. breast carcinoma
- Immunoediting describes the theory that our immune system prevents many cancers. Which of the following is not one of its 3 phases (called the 3’e’s)?
a. efficiency
b. equilibrium
c. escape
d. elimination
a. efficiency
- Tumor-associated transplantation antigens (TAAs) are not found in:
a. fetal cells
b. tumor cells
c. bacterial cells
d. viral cells
c. bacterial cells
- The presence of HBsAg, anti-HBc and often HBeAg is characteristic of:
a. early acute phase HBV hepatitis
b. early convalescent phase HBV hepatitis
c. recovery phase of acute HBV hepatitis
d. past HBV infection
a. early acute phase HBV hepatitis
- From the test results in the table, it can be concluded that patient #3 has:
a. recent acute hepatitis A
b. acute hepatitis B
c. acute hepatitis C (non-A/non-B hepatitis)
d. chronic hepatitis B
b. acute hepatitis B
- The disappearance of HBsAg and HBeAg, the persistence of anti-HBc, the appearance of anti-HBs, and often of anti-HBe indicate:
a. early acute HBV hepatitis
b. early convalescent phase HBV hepatitis
c. recovery phase of acute HBV hepatitis
d. carrier state of acute HBV hepatitis
c. recovery phase of acute HBV hepatitis
- An example of a live attenuated vaccine used for human immunization is:
a. rabies
b. tetanus
c. hepatitis B
d. measles
d. measles
- What assay would confirm the immune status of hepatitis B Virus?
a. HBsAg
b. anti-HBs
c. IgM anti-HBcAg
d. hepatitis C Ag
b. anti-HBs