Anatomy
1 questionsT cells in lymph node are present in:
NEET-PG 2013 - Anatomy NEET-PG Practice Questions and MCQs
Question 701: T cells in lymph node are present in:
- A. Paracortical area (Correct Answer)
- B. Mantle layer
- C. Medullary cords
- D. Cortical follicles
Explanation: ***Paracortical area*** - The **paracortical area** contains a high concentration of **T cells**, particularly activated T cells in response to antigenic stimulation [1]. - It plays a crucial role in **immune responses**, bridging the cortex and medulla of the lymph node [1]. *Mantle layer* - The **mantle layer** surrounds the follicles and primarily consists of **B cells**, not T cells. - It is involved in the initial immune response but does not contain a significant number of T lymphocytes. *Medullary cords* - **Medullary cords** mainly contain **plasma cells** and macrophages, with very few T cells present. - Their primary function is the secretion of antibodies rather than T cell activation or response. *Cortical follicles* - **Cortical follicles** are primarily sites for **B cell activation and proliferation**. - While they may have some T cells at their periphery, the majority of T cells are located in the paracortical area.
Biochemistry
2 questionsWhat is the number of variable regions present on each light and heavy chain of an antibody?
Which immunoglobulin is known to be heat-labile?
NEET-PG 2013 - Biochemistry NEET-PG Practice Questions and MCQs
Question 701: What is the number of variable regions present on each light and heavy chain of an antibody?
- A. 1 (Correct Answer)
- B. 2
- C. 3
- D. 4
Explanation: ***1*** - Each **light chain** and **heavy chain** within an antibody molecule contains **one variable region (V domain)**. - These variable regions are crucial for **antigen binding specificity**, as they combine to form the antigen-binding site. - The variable domain is located at the **N-terminal end** of each chain. *2* - While a complete antibody molecule has **two antigen-binding sites** (bivalent), each formed by pairing of VH and VL domains, individual chains possess only **one variable region each**. - The number '2' refers to the total number of identical binding sites on the intact antibody, not the number of variable regions per chain. *3* - The number **3** does not correspond to the number of variable regions on individual chains. - This might be confused with the **three complementarity-determining regions (CDRs)** present within each variable domain (CDR1, CDR2, CDR3), which are hypervariable loops that directly contact the antigen. *4* - The number **4** is incorrect for variable regions. - This number corresponds to the total number of **polypeptide chains** in a complete IgG antibody (2 heavy + 2 light chains), or the number of **constant domains** in some heavy chain isotypes (IgM, IgE have 4 CH domains).
Question 702: Which immunoglobulin is known to be heat-labile?
- A. IgA
- B. IgG
- C. IgM (Correct Answer)
- D. IgE
Explanation: ***IgM*** - **IgM** is known for its **heat lability** and is readily denatured at 56°C within a few minutes. - This characteristic is due to its **pentameric structure** held together by disulfide bonds and J chains, which are sensitive to thermal denaturation. - Heat lability of IgM is clinically important in complement fixation tests and other laboratory assays where heat inactivation is performed. - IgM is the first antibody produced in primary immune response and its heat sensitivity distinguishes it from other immunoglobulins. *IgA* - **IgA** exists in monomeric (serum) and dimeric (secretory) forms and shows moderate stability to heat. - Secretory IgA is relatively stable as it needs to function in harsh mucosal environments, though not as heat-resistant as IgG. - Does not exhibit the pronounced heat lability characteristic of IgM. *IgG* - **IgG** is the most stable immunoglobulin and is highly resistant to heat denaturation. - Can withstand temperatures up to 60-70°C without significant loss of activity. - Its monomeric structure with strong intramolecular bonds provides exceptional thermal stability. - Most abundant antibody in serum and has the longest half-life. *IgE* - **IgE** is actually quite stable to heat and can withstand 56°C for extended periods. - While it has a short half-life in serum (2-3 days), this is due to receptor binding rather than heat instability. - Important in type I hypersensitivity reactions and parasitic infections. - Does not show the characteristic heat lability that defines IgM.
Microbiology
5 questionsMacrophage tropic strains of HIV use which co-receptor?
How many segments of RNA does the Influenza virus have?
Prions are best killed by
What are the changes in the variable region of immunoglobulins?
All are true regarding the development of T-cells, except?
NEET-PG 2013 - Microbiology NEET-PG Practice Questions and MCQs
Question 701: Macrophage tropic strains of HIV use which co-receptor?
- A. CCR5 (Correct Answer)
- B. CXCR4
- C. CCR3
- D. CCR2
Explanation: ***CCR5*** - **Macrophage-tropic** HIV strains, also known as **R5 strains**, primarily use the **CCR5 co-receptor** to enter target cells. - These strains are typically involved in the **initial infection** and transmission of HIV. - CCR5-tropic viruses are usually the **predominant strains transmitted** during sexual transmission. *CXCR4* - **T-cell-tropic** HIV strains, or **X4 strains**, preferentially utilize the **CXCR4 co-receptor** for cell entry. - These strains are associated with a **more rapid decline in CD4+ T-cell counts** during later stages of HIV infection. - Emergence of X4 strains is linked to **disease progression**. *CCR3* - While a chemokine receptor, **CCR3** is not a primary co-receptor used by common HIV strains for entry into macrophages or T cells. - CCR3 is primarily involved in **eosinophil chemotaxis** and allergic responses. *CCR2* - **CCR2** is another chemokine receptor but is **not a major co-receptor** for HIV entry. - While some laboratory-adapted strains may show minor usage, it is not clinically significant for macrophage-tropic HIV strains.
Question 702: How many segments of RNA does the Influenza virus have?
- A. 5 segments of single-stranded RNA
- B. 8 segments of double-stranded DNA
- C. 8 segments of single-stranded DNA
- D. 8 segments of single-stranded RNA (Correct Answer)
Explanation: ***8 segments of single-stranded RNA*** - The **Influenza virus** is characterized by its segmented genome, which consists of **eight distinct negative-sense single-stranded RNA (ssRNA)** molecules. - This segmentation is crucial for its high mutation rate and ability to undergo **antigenic shift** and **antigenic drift**, leading to new strains. *5 segments of single-stranded RNA* - This option is incorrect because the Influenza virus specifically has **eight segments**, not five. - While it is a single-stranded RNA virus, the number of segments is a key characteristic. *8 segments of double-stranded DNA* - This option is incorrect as Influenza is an **RNA virus**, not a DNA virus, and its genetic material is single-stranded, not double-stranded. - No known influenza viruses have a **double-stranded DNA genome**. *8 segments of single-stranded DNA* - This option is incorrect because Influenza is an **RNA virus**, not a DNA virus. - Its genetic material is composed of **RNA**, specifically negative-sense single-stranded RNA.
Question 703: Prions are best killed by
- A. Incineration at high temperatures
- B. Autoclaving at 134°C (for 18 minutes) (Correct Answer)
- C. 5% formalin solution
- D. Sodium hypochlorite solution
Explanation: ***Autoclaving at 134°C (for 18 minutes)*** - **Prions** are highly resistant to conventional sterilization methods, and **autoclaving at 134°C for at least 18 minutes** is the **most effective method for sterilizing reusable medical instruments** contaminated with prions. - This high temperature and pressure protocol (WHO/CDC recommended) helps to denature the misfolded protein structure of prions, reducing their infectivity to safe levels. - **In the context of sterilization and disinfection**, this is the best practical method for surgical instruments that cannot be discarded. *Incineration at high temperatures* - **Incineration at 800-1000°C** achieves complete combustion and is **highly effective** at destroying prions. - However, incineration is used only for **single-use disposable items** and prion-contaminated waste, not for reusable surgical instruments. - In the clinical context of sterilization (implied by this topic), autoclaving is the preferred answer as it applies to reusable equipment. *Sodium hypochlorite solution* - **Sodium hypochlorite** (bleach) at **high concentrations** (20,000 ppm or 2% available chlorine) for extended contact times (1+ hours) can inactivate prions. - However, it is **corrosive to instruments**, damages tissue samples, and requires precise concentration and exposure conditions, making it less practical than autoclaving. *5% formalin solution* - Formalin is **not effective at inactivating prions**; it can actually **preserve and stabilize** prion infectivity. - Formalin cross-links proteins and preserves tissue morphology but does not reliably break down the highly stable **beta-sheet structures** characteristic of prions.
Question 704: What are the changes in the variable region of immunoglobulins?
- A. Isotype
- B. Epitope
- C. Allotype
- D. Idiotype (Correct Answer)
Explanation: ***Idiotype*** - **Idiotype** refers to the unique set of antigenic determinants in the **variable region** of an antibody molecule, specifically within the **hypervariable regions (complementarity-determining regions, CDRs)**. - These unique determinants allow antibodies to recognize specific antigens and are generated by the specific **V(D)J gene rearrangements** in B cells. *Isotype* - **Isotype** refers to the constant region of an antibody, determining its class (e.g., **IgG, IgM, IgA, IgD, IgE**). - This region defines the antibody's effector functions and has nothing to do with the antigen-binding variability. *Allotype* - **Allotype** refers to minor genetic variations within the **constant region** of an antibody molecule within a species. - These variations are due to different alleles inherited from parents and are not associated with the variable region that binds to antigens. *Epitope* - An **epitope** is the specific part of an **antigen** that an antibody or T-cell receptor recognizes and binds to. - It is a feature of the antigen, not a change within the variable region of the immunoglobulin itself.
Question 705: All are true regarding the development of T-cells, except?
- A. T-cells are formed in bone marrow
- B. In lymph nodes, T-cells are found in paracortical area
- C. Maturation of T-cells take place in thymus
- D. T-cells are located in mantle layer of spleen (Correct Answer)
Explanation: ***T-cells are located in mantle layer of spleen*** - The **mantle layer** (or marginal zone) of the spleen is primarily associated with **B-lymphocytes**, which are involved in antibody production. - While T-cells are present in the spleen, they are predominantly found in the **periarteriolar lymphoid sheath (PALS)**, which is part of the white pulp, rather than the mantle layer. *T-cells are formed in bone marrow* - **Hematopoietic stem cells** in the **bone marrow** are the progenitors of all blood cells, including lymphocytes. - These stem cells differentiate into **lymphoid stem cells**, which then travel to the thymus to become T-cells. *Maturation of T-cells take place in thymus* - **T-cell precursors** migrate from the bone marrow to the **thymus**, where they undergo a complex process of differentiation and selection. - In the thymus, T-cells acquire their **T-cell receptors (TCRs)** and undergo positive and negative selection to ensure they are self-MHC restricted and tolerant to self-antigens. *In lymph nodes, T-cells are found in paracortical area* - The **paracortical area** (or paracortex) of the lymph node is the **T-cell zone**, rich in T-lymphocytes and dendritic cells. - This region is crucial for the interaction between T-cells and antigen-presenting cells, initiating adaptive immune responses.
Pediatrics
1 questionsAt what age does clinically significant IgG production begin?
NEET-PG 2013 - Pediatrics NEET-PG Practice Questions and MCQs
Question 701: At what age does clinically significant IgG production begin?
- A. Around 6 months (Correct Answer)
- B. Around 1 year
- C. Around 2 years
- D. Around 3 years
Explanation: ***Around 6 months*** - Maternal IgG levels, which provide **passive immunity**, decrease significantly by 3-6 months of age. - Infants begin to produce their own **clinically significant** levels of IgG around this time, coinciding with the "physiologic nadir" of IgG. *Around 1 year* - While IgG production continues to mature, significant production has already begun by 6 months to replace declining maternal antibodies. - By 1 year, the immune system is more robust, but the initial critical transition occurs earlier. *Around 2 years* - By this age, children generally have a robust adaptive immune response, and the period of vulnerability due to low IgG has passed. - This option is too late for the beginning of clinically significant IgG production. *Around 3 years* - This age is far past the point where children start producing their own significant levels of IgG. - The immune system is well-developed by 3 years, and initial IgG production started much earlier.
Physiology
1 questionsWhich immunoglobulin is primarily secreted by the intestine?
NEET-PG 2013 - Physiology NEET-PG Practice Questions and MCQs
Question 701: Which immunoglobulin is primarily secreted by the intestine?
- A. IgG
- B. IgM
- C. IgA (Correct Answer)
- D. IgD
Explanation: **IgA** - **Secretory IgA** is the dominant immunoglobulin in mucosal secretions, including those of the intestine. - It plays a crucial role in providing **local immunity** by preventing microbial adherence and neutralizing toxins on mucosal surfaces. *IgG* - **IgG** is the most abundant immunoglobulin in serum and plays a major role in systemic immunity, including opsonization and complement activation. - While some IgG is found in secretions, it is not the primary immunoglobulin secreted by the intestine. *IgM* - **IgM** is a pentameric immunoglobulin, primarily found in blood and lymph, where it is very effective in activating the complement system and agglutinating antigens. - Although it can be found at mucosal surfaces in small amounts, it is not the principal secreted antibody in the intestine. *IgD* - **IgD** is primarily found on the surface of naive B lymphocytes, where it functions as a B cell receptor. - Its role in secreted form is minimal, and it is not significantly secreted into the intestine or other bodily fluids.