Nokea
Which of the following statements is NOT true
- A. Light chains isotypes are functionally different
- B. The antigen binding site of a B cell receptor is identical to the antigen binding site of antibodies secreted by the same B cell
- C. Both heavy and light chain domains assume a compact barrel structure
- D. The hinge region assumes a more open and flexible structure
Correct Answer: A
Rationale: The correct answer is A: Light chains isotypes are functionally different. This statement is NOT true because light chain isotypes (kappa and lambda) have distinct primary structures but serve the same function in antigen binding. The heavy chain determines the effector function of antibodies. The other choices are correct: B) The antigen binding site of a B cell receptor is identical to the antigen binding site of antibodies secreted by the same B cell, as both use the same variable regions for antigen recognition. C) Both heavy and light chain domains assume a compact barrel structure, which is essential for antibody stability and function. D) The hinge region assumes a more open and flexible structure, allowing antibodies to bind antigens at different orientations.
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In mice, mutations of which of the following genes cause the 'scurfy' phenotype (scaly skin and multiple autoimmune disorders)?
- A. FOXP3
- B. AIRE
- C. NFkB
- D. IRF
Correct Answer: A
Rationale: Rationale:
1. FOXP3 gene encodes a transcription factor crucial for regulatory T cells function.
2. Mutations in FOXP3 lead to dysfunctional regulatory T cells, causing autoimmune disorders.
3. Scurfy phenotype matches the symptoms of autoimmune disorders seen with FOXP3 mutations.
Summary:
- B (AIRE): AIRE mutations cause autoimmune polyendocrine syndrome, not scurfy phenotype.
- C (NFkB): NFkB is a transcription factor involved in immune response but not linked to scurfy phenotype.
- D (IRF): IRF is a regulator of interferon signaling, not directly associated with scurfy phenotype.
Which of the following is necessary to produce a T-cell repertoire capable of interacting with self MHC molecules?
- A. Two of these responses are correct
- B. Positive selection
- C. Negative selection
- D. Induction of energy
Correct Answer: B
Rationale: Positive selection is necessary to produce a T-cell repertoire capable of interacting with self MHC molecules. During positive selection in the thymus, T-cells that can recognize self MHC molecules are retained, ensuring self-tolerance and functionality. Negative selection eliminates self-reactive T-cells. Induction of anergy is a state of T-cell unresponsiveness and does not contribute to the development of a functional T-cell repertoire. Choice A is incorrect as only positive selection is necessary for self MHC recognition.
Why do opportunistic diseases develop in an individual with AIDS?
- A. They are side effects of drug treatment of AIDS.
- B. They are sexually transmitted to individuals during exposure to HIV.
- C. They are characteristic in individuals with stimulated B and T lymphocytes.
- D. These infections or tumors occur in a person with an incompetent immune system.
Correct Answer: D
Rationale: Opportunistic diseases arise because the immune system is severely compromised in individuals with AIDS, making them susceptible to infections and cancers they would otherwise resist.
Why don't we have a successful HIV vaccine?
- A. The high mutation rate of HIV interferes with the generation of a protective memory response
- B. Because it is difficult to induce mucosal immunity that would block the sexual transmission of the virus
- C. Because HIV targets immune cells
- D. All of the above represent challenges for the creation of an effective HIV vaccine
Correct Answer: D
Rationale: The correct answer is D because all the statements in choices A, B, and C are valid reasons why we don't have a successful HIV vaccine.
A: HIV has a high mutation rate, making it challenging to generate a protective memory response.
B: Inducing mucosal immunity is difficult to block sexual transmission, a common route of HIV infection.
C: HIV targets immune cells, which hinders the immune system's ability to mount an effective response.
Therefore, all these factors combined pose significant challenges for creating an effective HIV vaccine.
Which antibodies are involved in Type II hypersensitivity?
- A. IgE and IgA
- B. IgG and IgM
- C. IgD and IgG
- D. IgM and IgA
Correct Answer: B
Rationale: The correct answer is B (IgG and IgM) because in Type II hypersensitivity, antibodies target antigens on cell surfaces or tissues. IgG and IgM antibodies are involved in this type of immune response by binding to antigens and triggering cell destruction through complement activation or phagocytosis. IgE and IgA (choice A) are typically associated with Type I and Type III hypersensitivity, respectively. IgD (choice C) is primarily involved in B cell activation, while IgA (choice D) is more commonly associated with mucosal immunity.