Publications by authors named "Alexandre Nouel"

Article Synopsis
  • - HIV elite controllers possess CD4 + T cells that are highly effective in recognizing and responding to Gag antigens, which may help them resist HIV infection and depletion.
  • - These controllers demonstrate advanced Th1 differentiation patterns, but show reduced levels of the CCR5 marker compared to treated patients, indicating a lower susceptibility to HIV entry.
  • - Some controllers have genetic mutations that further limit CCR5 expression, while others may downregulate it functionally through interactions with high-avidity antigens, suggesting both genetic and functional mechanisms promote natural HIV control.
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Rare patients who spontaneously control HIV replication provide a useful model to inform HIV vaccine development. HIV controllers develop particularly efficient antiviral CD4 T cell responses mediated by shared high-affinity TCRs. To determine whether the candidate DNA vaccine ADVAX could induce similar responses, we analyzed Gag-specific primary CD4 T cells from healthy volunteers who received ADVAX DNA by electroporation.

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The rare patients who are able to spontaneously control HIV replication in the absence of therapy show signs of a particularly efficient cellular immune response. To identify the molecular determinants that underlie this response, we characterized the T cell receptor (TCR) repertoire directed at Gag293, the most immunoprevalent CD4 epitope in the HIV-1 capsid. HIV controllers from the ANRS CODEX cohort showed a highly skewed TCR repertoire that was characterized by a predominance of TRAV24 and TRBV2 variable genes, shared CDR3 motifs, and a high frequency of public clonotypes.

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Transplantation is the preferred treatment for most end-stage solid organ diseases. Despite potent immunosuppressive agents, chronic rejection remains a real problem in transplantation. For many years, the predominant immunological focus of research into transplant rejection has been T cells.

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In kidney transplantation, the composition of the B-cell compartment is increasingly identified as an important determinant for graft outcome. Whereas naive and transitional B cells have been associated with long-term allograft survival and operational tolerance, memory B cells have been linked to graft rejection and graft loss. Chronic antibody-mediated rejection now represents a major complication in transplantation and is a challenge in current therapeutics.

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