TY - JOUR
T1 - The T-cell-independent immune response to the hapten NP uses a large repertoire of heavy chain genes
AU - Maizels, Nancy
AU - Bothwell, Alfred
N1 - Funding Information:
We thank Dean Ballard, Peter Blier, Kim Bottomly, Charlie Janeway, and Alan Weiner for helpful discussions and comments on this manuscript. Marcy Bothwell, Karen Chorney, and Patricia Pace provided excellent technical assistance. This work was supported by the Howard Hughes Medical Institute.
PY - 1985/12
Y1 - 1985/12
N2 - Hybridomas generated from C57BL/6 mice immunized with the hapten NP coupled to ficoll, a T-cell-independent carrier, produce monoclonal antibodies that use a large repertoire of VH regions and light chains. This contrasts with the homogeneity of the strain-specific response to NP observed with T-cell-dependent carriers, where most of the antibodies use a single VH region, V186.2, in combination with the lambda-1 light chain. There is no evidence for somatic mutation in any of the sequenced regions of the antibodies generated by NP-ficoll. Thus T cell participation is required for the homogeneity of the strain-specific hapten response, and probably for somatic mutation as well.
AB - Hybridomas generated from C57BL/6 mice immunized with the hapten NP coupled to ficoll, a T-cell-independent carrier, produce monoclonal antibodies that use a large repertoire of VH regions and light chains. This contrasts with the homogeneity of the strain-specific response to NP observed with T-cell-dependent carriers, where most of the antibodies use a single VH region, V186.2, in combination with the lambda-1 light chain. There is no evidence for somatic mutation in any of the sequenced regions of the antibodies generated by NP-ficoll. Thus T cell participation is required for the homogeneity of the strain-specific hapten response, and probably for somatic mutation as well.
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U2 - 10.1016/0092-8674(85)90244-2
DO - 10.1016/0092-8674(85)90244-2
M3 - Article
C2 - 2416469
AN - SCOPUS:0022297171
SN - 0092-8674
VL - 43
SP - 715
EP - 720
JO - Cell
JF - Cell
IS - 3 PART 2
ER -