Abstract

The contribution of the λ-light chain to the development of peripheral B cell repertoire and generation of specific antibodies to haptens and polysaccharide antigens was studied in genetically manipulated kappa-deficient and λ 2-transgenic mice. The results clearly demonstrate a non-stoichiometric V H gene family expression in the absence of k-light chain and suggest a non-stochastic pairing between V H and V λ genes, expressed in the peripheral B cell repertoire. A shift in V H gene utilization in the case of Vl λ + antibodies was evident in response to β2–6 fructosan and TNP hapten. These observations demonstrate the availability of compensatory mechanisms in the absence of V K genes and are consistent with the hypothesis that V H gene family expression is controlled by genetic factors from inside the V H locus. Furthermore, genetic factors from outside the V H locus, namely restricted available light chain diversity, may lead to a shift in V H gene utilization in the peripheral B cell repertoire.

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