TY - JOUR
T1 - Treatment with native heterodimeric IL-15 increases cytotoxic lymphocytes and reduces SHIV RNA in lymph nodes
AU - Watson, Dionysios C.
AU - Moysi, Eirini
AU - Valentin, Antonio
AU - Bergamaschi, Cristina
AU - Devasundaram, Santhi
AU - Fortis, Sotirios P.
AU - Bear, Jenifer
AU - Chertova, Elena
AU - Bess, Julian
AU - Sowder, Ray
AU - Venzon, David J.
AU - Deleage, Claire
AU - Estes, Jacob D.
AU - Lifson, Jeffrey D.
AU - Petrovas, Constantinos
AU - Felber, Barbara K.
AU - Pavlakis, George N.
N1 - Publisher Copyright:
© 2018 Library of Science. All Rights Reserved.
PY - 2018/2
Y1 - 2018/2
N2 - B cell follicles in secondary lymphoid tissues represent an immune privileged sanctuary for AIDS viruses, in part because cytotoxic CD8+T cells are mostly excluded from entering the follicles that harbor infected T follicular helper (TFH) cells. We studied the effects of native heterodimeric IL-15 (hetIL-15) treatment on uninfected rhesus macaques and on macaques that had spontaneously controlled SHIV infection to low levels of chronic viremia. hetIL-15 increased effector CD8+T lymphocytes with high granzyme B content in blood, mucosal sites and lymph nodes, including virus-specific MHC-peptide tetramer+ CD8+cells in LN. Following hetIL-15 treatment, multiplexed quantitative image analysis (histo-cytometry) of LN revealed increased numbers of granzyme B+T cells in B cell follicles and SHIV RNA was decreased in plasma and in LN. Based on these properties, hetIL-15 shows promise as a potential component in combination immunotherapy regimens to target AIDS virus sanctuaries and reduce long-term viral reservoirs in HIV-1 infected individuals.
AB - B cell follicles in secondary lymphoid tissues represent an immune privileged sanctuary for AIDS viruses, in part because cytotoxic CD8+T cells are mostly excluded from entering the follicles that harbor infected T follicular helper (TFH) cells. We studied the effects of native heterodimeric IL-15 (hetIL-15) treatment on uninfected rhesus macaques and on macaques that had spontaneously controlled SHIV infection to low levels of chronic viremia. hetIL-15 increased effector CD8+T lymphocytes with high granzyme B content in blood, mucosal sites and lymph nodes, including virus-specific MHC-peptide tetramer+ CD8+cells in LN. Following hetIL-15 treatment, multiplexed quantitative image analysis (histo-cytometry) of LN revealed increased numbers of granzyme B+T cells in B cell follicles and SHIV RNA was decreased in plasma and in LN. Based on these properties, hetIL-15 shows promise as a potential component in combination immunotherapy regimens to target AIDS virus sanctuaries and reduce long-term viral reservoirs in HIV-1 infected individuals.
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U2 - 10.1371/journal.ppat.1006902
DO - 10.1371/journal.ppat.1006902
M3 - Article
C2 - 29474450
AN - SCOPUS:85042729001
SN - 1553-7366
VL - 14
JO - PLoS Pathogens
JF - PLoS Pathogens
IS - 2
M1 - e1006902
ER -