High diversity of the immune repertoire in humanized NOD.SCID.γc−/− mice

G Marodon, D Desjardins, L Mercey… - European journal of …, 2009 - Wiley Online Library
G Marodon, D Desjardins, L Mercey, C Baillou, P Parent, M Manuel, C Caux, B Bellier
European journal of immunology, 2009Wiley Online Library
The diversity of the human immune repertoire and how it relates to a functional immune
response has not yet been studied in detail in humanized NOD. SCID. γc−/−
immunodeficient mice. Here, we used a multiplex PCR on genomic DNA to quantify the
combinatorial diversity of all possible V–J rearrangements at the TCR‐β chain and heavy
chain Ig locus. We first show that the combinatorial diversity of the TCR‐β chain generated in
the thymus was well preserved in the periphery, suggesting that human T cells were not …
Abstract
The diversity of the human immune repertoire and how it relates to a functional immune response has not yet been studied in detail in humanized NOD.SCID.γc−/− immunodeficient mice. Here, we used a multiplex PCR on genomic DNA to quantify the combinatorial diversity of all possible V–J rearrangements at the TCR‐β chain and heavy chain Ig locus. We first show that the combinatorial diversity of the TCR‐β chain generated in the thymus was well preserved in the periphery, suggesting that human T cells were not vastly activated in mice, in agreement with phenotypic studies. We then show that the combinatorial diversity in NOD.SCID.γc−/− mice reached 100% of human reference samples for both the TCR and the heavy chain of Ig. To document the functionality of this repertoire, we show that a detectable but weak HLA‐restricted cellular immune response could be elicited in reconstituted mice after immunization with an adenoviral vector expressing HCV envelope glycoproteins. Altogether, our results suggest that humanized mice express a diversified repertoire and are able to mount antigen‐specific immune responses.
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