Nokea
The major role of the complement system is to work in conjunction with
- A. antibodies to lyse cells via the C8 and C9 components
- B. the major histocompatibility complex for cell recognition
- C. antibodies to opsonize cells
- D. the T-cell receptor for production of lymphokines
Correct Answer: A
Rationale: Rationale: The complement system is a group of proteins that enhance the ability of antibodies and phagocytic cells to clear pathogens. Choice A is correct because the C8 and C9 components of the complement system form the membrane attack complex which lyses cells. Choices B, C, and D are incorrect because the complement system primarily functions independently of the major histocompatibility complex, antibodies for opsonization, and T-cell receptor for lymphokine production.
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What is the medical term for excessive bleeding?
- A. Thrombosis
- B. Embolus
- C. Hemorrhage
- D. Hemostasis
Correct Answer: C
Rationale: The correct answer is C: Hemorrhage. Hemorrhage refers to excessive bleeding. Thrombosis (A) is the formation of blood clots, not excessive bleeding. Embolus (B) is a blood clot that travels through the bloodstream and blocks a blood vessel. Hemostasis (D) is the process of stopping bleeding, not the term for excessive bleeding. In summary, only choice C directly relates to the medical term for excessive bleeding.
Defensins are
- A. Released by mast cells during an allergic reaction
- B. Membrane-disrupting peptides
- C. Acute phase proteins
- D. Opsonins
Correct Answer: B
Rationale: The correct answer is B: Membrane-disrupting peptides. Defensins are antimicrobial peptides that disrupt bacterial cell membranes. This disrupts the integrity of the bacterial cell, leading to cell lysis and death. Choice A is incorrect because mast cells release histamines, not defensins. Choice C is incorrect as acute phase proteins are involved in the immune response to inflammation. Choice D is incorrect as opsonins are molecules that enhance phagocytosis of pathogens by immune cells.
In the 1960s, smallpox was endemic:
- A. In many developing countries
- B. In North America
- C. In England
- D. Globally
Correct Answer: A
Rationale: The correct answer is A: In many developing countries. Smallpox was indeed endemic in many developing countries in the 1960s, causing significant morbidity and mortality. This is supported by historical records and epidemiological data from that time period. Choices B, C, and D are incorrect because smallpox was not endemic in North America, England, or globally during the 1960s. Smallpox eradication efforts led to the global eradication of the disease in 1980, but in the 1960s, it was still prevalent in many developing countries.
Which of the following is not a systemic cytokine?
- A. TNF
- B. IL-1
- C. IL-6
- D. IL-8
Correct Answer: D
Rationale: The correct answer is D: IL-8. IL-8 is not a systemic cytokine because it mainly acts locally at the site of inflammation to recruit neutrophils. Systemic cytokines like TNF, IL-1, and IL-6 have widespread effects throughout the body, influencing various immune responses and inflammatory processes. IL-8's localized action distinguishes it from systemic cytokines, making it the correct choice. TNF, IL-1, and IL-6 are all systemic cytokines that play key roles in regulating the immune response and inflammation at a systemic level, unlike IL-8.
Which T cell type helps activate B cells?
- A. Cytotoxic T cells
- B. Helper T cells
- C. Regulatory T cells
- D. Memory T cells
Correct Answer: B
Rationale: The correct answer is B: Helper T cells. Helper T cells play a crucial role in activating B cells by releasing cytokines that stimulate B cell proliferation and differentiation into plasma cells, which produce antibodies. Cytotoxic T cells (A) are involved in directly killing infected cells. Regulatory T cells (C) suppress immune responses. Memory T cells (D) are responsible for maintaining immunological memory for future responses. Thus, Helper T cells are the key cell type that helps activate B cells.