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Integral University 2011 M.Tech Biotechnology Immunotechnology - exam paper

Wednesday, 23 January 2013 06:25Web



No. of Printed Pages - 3    MTBT-302(A)

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Roll No. !

M. Tech.

THIRD SEMESTER EXAMINATION, 2011-12

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IMMUNOTECHNOLOGY

Time : 3 Hours    Total Marks : 100

Note : (i) Attempt any FIVE questions.

(ii) Marks are indicated against each question.

(a) Answer the following :    2x5 = 10

(i)    The single best chance of a tissue graft being accepted in a

human recipient is if it is :

A.     An isograft

B.    An allograft given under the cover of potent immunosuppression.

C.    A xenograft from a pig in which the gene fro alpha-1, 3-galactosyltransferase has been knocked-out and therefore the Gal epitope eliminated.

D.    Given to a recipient that is treated with anti-CD3.

(ii)    Each of the following statements concerning a hybridoma

cell is correct EXCEPT :

A.    The spleen cell component provides the ability to form antibody.

B.    The myeloma cell component provides the ability to grow indefinitely.

C.    The antibody produced by a hybridoma cell is IgM, because heavy-chain switching does not occur.

D.    The antibody produced by a hybridoma cell is homogeneous; i.e. it is directed against a single epitope.

1    P.T.O.

MTBT-302(A)

(Hi) Which one of the following is the BEST method of reducing the effect of graft-versus-host disease in a bone marrow recipient?

A.    Matching the complement components of donor and recipient.

B.    Administering alpha interferon

C.    Removing mature T cells from the graft

D.    Removing pre-B cells from the graft

(iv)    Graft and tumor rejection are mediated primarily by :

A.    Non-complement-fixing antibodies

B.    Phagocytic cells

C.    Helper T cells

D.    Cytotoxic T cells

(v)    A patient with severe asthma suffers due to high level of histamines. The best treatment strategy suggested is :

A.    Monoclonal antibodies against IgE

B.    Corticosteroidal drugs

C.    Recombinant IL-4

D.    All of the above.

(b) Give a brief account on :    2x5 = 10

(i) Chimeric toxins (ii) X-linked agammaglobulinemia

(iii) Adjuvants    J]v) Xenograft

(v) Serotyping

2. (a) Give a detailed account on mechanism adopted by the HIV virus to infect CD4+T cells.    10

(b) Describe the immune evasion mechanism adopted by the virus to establish itself.    10

MTBT-302(A)

3 Write short notes on any Two of the following :    10 x 2 = 20

(a) DNA vaccines    (ii) Stem cell therapy

(c)    IL-12

4. Differentiate between the following :    5 x 4 = 20

(a) TATA and TSTA J Killed and Attenuated vaccines Active and Passive therapy

(d)    Chimeric and humanized mtpnoclonal antibodies

5. Describe in detail the basic biology of Type I and Type II interferons and also mention their therapeutic potential.    20

6 Give a detailed protocol of production of mouse monoclonal antibody against lL-2 receptor and also mention its use as a therapeutic agent. 20

OR

Give a detailed account on corticosteroidal and non steroidal drugs and their mechanism of action as anti-inflammatory agents.    20

7 Comment the following :    4 x 5 = 20

( ELISA

(W Hyperacute rejection

(c)    IL-20

(d)    Antimetabolites

(e)    Peptide therapy

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