Broadly targeted CD8 + T cell responses restricted by major histocompatibility complex E

Author:

Hansen Scott G.1,Wu Helen L.1,Burwitz Benjamin J.1,Hughes Colette M.1,Hammond Katherine B.1,Ventura Abigail B.1,Reed Jason S.1,Gilbride Roxanne M.1,Ainslie Emily1,Morrow David W.1,Ford Julia C.1,Selseth Andrea N.1,Pathak Reesab1,Malouli Daniel1,Legasse Alfred W.1,Axthelm Michael K.1,Nelson Jay A.1,Gillespie Geraldine M.2,Walters Lucy C.2,Brackenridge Simon2,Sharpe Hannah R.2,López César A.3,Früh Klaus1,Korber Bette T.34,McMichael Andrew J.2,Gnanakaran S.3,Sacha Jonah B.1,Picker Louis J.1

Affiliation:

1. Vaccine and Gene Therapy Institute and Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR 97006, USA.

2. Nuffield Department of Medicine, University of Oxford, Oxford OX37FZ, UK.

3. Theoretical Biology and Biophysics Group, Los Alamos National Laboratory, Los Alamos, NM 87545, USA.

4. The New Mexico Consortium, Los Alamos, NM 87545, USA.

Abstract

An unconventional route to protection One promising approach toward an HIV-1 vaccine involves infecting people with cytomegalovirus engineered to express proteins from HIV-1. This approach, which works by eliciting virus-killing CD8 + T cells, provides robust protection in nonhuman primate models. Hansen et al. have found out why this approach is so effective. Normally, peptide antigens presented by major histocompatibility complex-1a (MHC-Ia) activate CD8 + T cells. In vaccinated monkeys, however, CD8 + T cells reacted to peptide antigens presented by MHC-E molecules instead. Moreover, MHC-E could present a much wider range of peptides than MHC-Ia. Science , this issue p. 714

Funder

NIH

Center for HIV/AIDS Vaccine Immunology and Immunogen Discovery

Bill and Melinda Gates Foundation

Aeras Global TB Vaccine Foundation

Los Alamos National Laboratory (LANL)

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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