Evidence map›Paper›PMID 28177966›Full record

ArticleJournal of acquired immune deficiency syndromes (1999)2017

High Number of Activated CD8+ T Cells Targeting HIV Antigens Are Present in Cerebrospinal Fluid in Acute HIV Infection.

Cari F Kessing, Serena Spudich, Victor Valcour, Pearline Cartwright, Thep Chalermchai, James L K Fletcher, Hiroshi Takata, Carmen Nichols, Benjamin J Josey, Bonnie Slike and 14 more

Abstract read
In one paragraph

Article in Journal of acquired immune deficiency syndromes (1999), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 39 citations in OpenAlex.

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  17. ΔJournal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2020
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  20. Neurosyphilis During Acute HIV Infection: A CNS Immunologic and Virologic Characterization.Journal of acquired immune deficiency syndromes (1999) · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors at 13 institutions in 4 countries.

Cari F Kessing*Vaccine and Gene Therapy Institute-Florida, Port St Lucie, FL; †Currently, Cari F. Kessing, Department of Immunology and Microbiology, The Scripps Research Institute, Jupiter, FL; Pearline Cartwright, Department of Epidemiology and Biostatistics, Case Western Reserve University School of Medicine, Cleveland, OH; Carmen Nichols and Benjamin J. Josey, Cell Therapies Institute, Nova Southeastern University, FL; ‡Yale University School of Medicine, New Haven, CT; §Memory and Aging Center, Department of Neurology, University of California, San Francisco, CA; ‖SEARCH, The Thai Red Cross AIDS Research Center, Bangkok, Thailand; ¶Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD; #U.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD; **University of Hawaii, Honolulu, HI; ††Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand; ‡‡Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden; and §§University College London Institute of Neurology, Queen Square, London, United Kingdom.
Serena Spudich
Victor Valcour
Pearline Cartwright
Thep Chalermchai
James L K Fletcher
Hiroshi Takata
Carmen Nichols
Benjamin J Josey
Bonnie Slike
Shelly J Krebs
Napapon Sailsuta
Sukalaya Lerdlum
Linda Jagodzinski
Somporn Tipsuk
Duanghathai Suttichom
Somprartthana Rattanamanee
Henrik Zetterberg
Joanna Hellmuth
Nittaya Phanuphak
Merlin L Robb
Nelson L Michael
Jintanat Ananworanich
Lydie Trautmann
Thai Red Cross Society · THWalter Reed Army Institute of Research · USHenry M. Jackson Foundation · USCase Western Reserve University · USChulalongkorn University · THScripps Research Institute · USUniversity College London · GBUniversity Memory and Aging Center · USUniversity of California, San Francisco · USUniversity of Hawaii System · USVaccine and Gene Therapy InstituteVaccine & Gene Therapy Institute of Florida · USYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
MOLECULAR BASIS OF VIRAL PATHOGENESIST32AI007354 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI DE LA TORRE, JUAN C. · 1989 to 2020
$5.2M
Preservation of adaptive immunity leads to HIV control upon treatment cessation.R01AI108433 · NIAID · VGTI FLORIDA · PI VASAN, SANDHYA · 2014 to 2018
$3.6M
Long-Term CNS Consequences of Treatment During Acute InfectionR01MH095613 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SPUDICH, SERENA S, VALCOUR, VICTOR · 2011 to 2015
$3.1M
Critical Role of Cytotoxic T Cells in HIV NeuropathogenesisR01MH106466 · NIMH · OREGON HEALTH & SCIENCE UNIVERSITY · PI PICKER, LOUIS J., SPUDICH, SERENA S · 2016 to 2020
$2.8M
Midcareer Mentoring Award for Patient-Oriented Research in HIV and CognitionK24MH098759 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VALCOUR, VICTOR · 2013 to 2017
$887k
Central Nervous System Effects in Acute HIV SeroconversionR21MH086341 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VALCOUR, VICTOR · 2009 to 2010
$367k
NCATS NIH HHS UL1 TR001863NIAID NIH HHS R01 AI108433NIAID NIH HHS T32 AI007354NIMH NIH HHS K24 MH098759NIMH NIH HHS R01 MH095613NIMH NIH HHS R01 MH106466NIMH NIH HHS R21 MH086341
6 · The paper itself

Abstract

backgroundCentral nervous system (CNS) infiltration by CD8 T cells is associated with neuroinflammation in many neurodegenerative diseases, including HIV-associated dementia. However, the role of CD8 T cells in the CNS during acute HIV infection (AHI) is unknown.

methodsWe analyzed the phenotype, gene expression, T cell receptor (TCR) repertoire, and HIV specificity of CD8 T cells in cerebrospinal fluid (CSF) of a unique cohort captured during the earliest stages of AHI (n = 26), chronic (n = 23), and uninfected (n = 8).

resultsCSF CD8 T cells were elevated in AHI compared with uninfected controls. The frequency of activated CSF CD8 T cells positively correlated to CSF HIV RNA and to markers of CNS inflammation. In contrast, activated CSF CD8 T cells during chronic HIV infection were associated with markers of neurological injury and microglial activation. CSF CD8 T cells in AHI exhibited increased functional gene expression profiles associated with CD8 T cells effector function, proliferation, and TCR signaling, a unique restricted TCR Vbeta repertoire and contained HIV-specific CD8 T cells directed to unique HIV epitopes compared with the periphery.

conclusionsThese results suggest that CSF CD8 T cells in AHI expanding in the CNS are functional and directed against HIV antigens. These cells could thus play a beneficial role protective of injury seen in chronic HIV infection if combination antiretroviral therapy is initiated early.

Indexed as

CD8-Positive T-LymphocytesCerebrospinal FluidHIV AntigensHIV InfectionsHumansImmunophenotypingT-Lymphocyte SubsetsHIV Antigens

Identifiers

PMID28177966
PMCPMC5388590
OpenAlexW2587309586

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.