RETRACTED: The protein LEM promotes CD8 + T cell immunity through effects on mitochondrial respiration
Author(s) -
Isobel Okoye,
Lihui Wang,
Katharina Pallmer,
Kirsten Richter,
Takahuru Ichimura,
Robert Haas,
Josh Crouse,
Onjee Choi,
Dean A. Heathcote,
Elena Lovo,
Claudio Mauro,
Reza Abdi,
Annette Oxenius,
Sophie Rutschmann,
Philip G. AshtonRickardt
Publication year - 2015
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aaa7516
Subject(s) - immunity , cd8 , biology , t cell , mitochondrion , t lymphocyte , gene , microbiology and biotechnology , mitochondrial dna , cellular immunity , cell metabolism , cell , immune system , genetics
Protective CD8(+) T cell-mediated immunity requires a massive expansion in cell number and the development of long-lived memory cells. Using forward genetics in mice, we identified an orphan protein named lymphocyte expansion molecule (LEM) that promoted antigen-dependent CD8(+) T cell proliferation, effector function, and memory cell generation in response to infection with lymphocytic choriomeningitis virus. Generation of LEM-deficient mice confirmed these results. Through interaction with CR6 interacting factor (CRIF1), LEM controlled the levels of oxidative phosphorylation (OXPHOS) complexes and respiration, resulting in the production of pro-proliferative mitochondrial reactive oxygen species (mROS). LEM provides a link between immune activation and the expansion of protective CD8(+) T cells driven by OXPHOS and represents a pathway for the restoration of long-term protective immunity based on metabolically modified cytotoxic CD8(+) T cells.
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