Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:3.4.22.36 (
caspase-1
)
6,285
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Antibody (Ab)-dependent cellular cytotoxicity (
ADCC
) is thought to potentially play a role in vaccine-induced protection from HIV-1. The characteristics of such antibodies remain incompletely understood. Furthermore, correlates between
ADCC
and HIV-1 immune status are not clearly defined. We screened the sera of 20 HIV-1-positive (HIV-1(+)) patients for
ADCC
. Normal human peripheral blood mononuclear cells were used to derive HIV-infected CD4(+) T cell targets and autologous, freshly isolated, natural killer (NK) cells in a novel assay that measures granzyme B (GrB) and HIV-1-infected CD4(+) T cell elimination (
ICE
) by flow cytometry. We observed that complex sera mediated greater levels of
ADCC
than anti-HIV-1 envelope glycoprotein (Env)-specific monoclonal antibodies and serum-mediated
ADCC
correlated with the amount of IgG and IgG1 bound to HIV-1-infected CD4(+) T cells. No correlation between
ADCC
and viral load, CD4(+) T cell count, or neutralization of HIV-1(SF162) or other primary viral isolates was detected. Sera pooled from clade B HIV-1(+) individuals exhibited breadth in killing targets infected with HIV-1 from clades A/E, B, and C. Taken together, these data suggest that the total amount of IgG bound to an HIV-1-infected cell is an important determinant of
ADCC
and that polyvalent antigen-specific Abs are required for a robust
ADCC
response. In addition, Abs elicited by a vaccine formulated with immunogens from a single clade may generate a protective
ADCC
response in vivo against a variety of HIV-1 species. Increased understanding of the parameters that dictate
ADCC
against HIV-1-infected cells will inform efforts to stimulate
ADCC
activity and improve its potency in vaccinees.
...
PMID:Antibody-dependent cellular cytotoxicity against primary HIV-infected CD4+ T cells is directly associated with the magnitude of surface IgG binding. 2267 85