Evidence map›Paper›PMID 26908875›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

CXCL13 is a plasma biomarker of germinal center activity.

Colin Havenar-Daughton, Madelene Lindqvist, Antje Heit, Jennifer E Wu, Samantha M Reiss, Kayla Kendric, Simon Bélanger, Sudhir Pai Kasturi, Elise Landais, Rama S Akondy and 14 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 238 papers.

0numbers the graph read from it
0cells of the map it votes in
238citing papers in PubMed
21.2field-weighted citation impact, top 1% 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

238 citing papers in PubMed, 351 citations in OpenAlex.

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  6. Protein/AS01Cell reports. Medicine · 2021
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  10. A pilot clinical trial of a near-infrared laser vaccine adjuvant: safety, tolerability, and cutaneous immune cell trafficking.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Trial
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  19. Aging restricts maturation of CXCL13bioRxiv : the preprint server for biology · 2026
    Article
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178 more citing papers are in PubMed but not listed here.

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 10 institutions in 2 countries.

Colin Havenar-DaughtonDivision of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037; Center for HIV/AIDS Vaccine Immunology and Immunogen Discovery, La Jolla, CA 92037;
Madelene LindqvistCenter for HIV/AIDS Vaccine Immunology and Immunogen Discovery, La Jolla, CA 92037; Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Boston, MA 02114;
Antje HeitCenter for HIV/AIDS Vaccine Immunology and Immunogen Discovery, La Jolla, CA 92037; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109;
Jennifer E WuDivision of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037;
Samantha M ReissDivision of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037;
Kayla KendricDivision of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037;
Simon BélangerDivision of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037;
Sudhir Pai KasturiYerkes National Primate Research Center, Emory University, Atlanta, GA 30322; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322;
Elise LandaisNeutralizing Antibody Center, International AIDS Vaccine Initiative, La Jolla, CA 92037;
Rama S AkondyEmory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322;ORCID http://orcid.org/0000-0003-4737-5240
Helen M McGuireDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94304;
Marcella BothwellDepartment of Surgery, University of California, San Diego, CA 92123; Pediatric Otolaryngology, Rady Children's Hospital-San Diego, San Diego, CA 92123;
Parsia A VagefiDepartment of Surgery, Massachusetts General Hospital, Boston, MA 02114;
Eileen ScullyRagon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Boston, MA 02114;
IAVI Protocol C Principal Investigators
Georgia D TomarasDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC 27710;
Mark M DavisDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94304; Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94304;
Pascal PoignardNeutralizing Antibody Center, International AIDS Vaccine Initiative, La Jolla, CA 92037; Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037;
Rafi AhmedCenter for HIV/AIDS Vaccine Immunology and Immunogen Discovery, La Jolla, CA 92037; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322;
Bruce D WalkerCenter for HIV/AIDS Vaccine Immunology and Immunogen Discovery, La Jolla, CA 92037; Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Boston, MA 02114; Howard Hughes Medical Institute, Chevy Chase, MD 20815;
Bali PulendranCenter for HIV/AIDS Vaccine Immunology and Immunogen Discovery, La Jolla, CA 92037; Yerkes National Primate Research Center, Emory University, Atlanta, GA 30322; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322;
M Juliana McElrathCenter for HIV/AIDS Vaccine Immunology and Immunogen Discovery, La Jolla, CA 92037; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109;
Daniel E KaufmannCenter for HIV/AIDS Vaccine Immunology and Immunogen Discovery, La Jolla, CA 92037; Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Boston, MA 02114; Department of Medicine, Université de Montréal, Montreal, QC H2X 0A9, Canada; Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Montreal, QC H2X 0A9, Canada.
Shane CrottyDivision of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037; Center for HIV/AIDS Vaccine Immunology and Immunogen Discovery, La Jolla, CA 92037; shane@lji.org.
International AIDS Vaccine Initiative · USLa Jolla Institute for Immunology · USEmory University · USScripps Research Institute · USDuke University · USHoward Hughes Medical Institute · USMassachusetts General Hospital · USRagon Institute of MGH, MIT and Harvard · USStanford University · USUniversity of California San Diego · US

Funding

LOC: HIV Vaccine Trials NetworkUM1AI068614 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Dan H. Barouch, Lawrence Corey · 2011 to 2026
$1175.6M
LC: HIV Vaccine Trials NetworkUM1AI068618 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Margaret Juliana McElrath · 2011 to 2026
$483.6M
Support Component D/Vaccine Discovery, Concept to ClinicUM1AI100663 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI BAROUCH, DAN H. · 2012 to 2018
$131.5M
Understanding the Role of Mucosal Antigen Presenting Cells in Regulating Immune ResponseR37AI048638 · NIAID · STANFORD UNIVERSITY · PI PULENDRAN, BALI · 2009 to 2018
$4.0M
Polarizing T Cell Responses in vivo With Dendritic CellsR37DK057665 · NIDDK · STANFORD UNIVERSITY · PI PULENDRAN, BALI · 2010 to 2019
$3.9M
NIAID NIH HHS R37 AI048638NIAID NIH HHS UM1 AI068614NIAID NIH HHS UM1 AI068618NIAID NIH HHS UM1 AI100663NIDDK NIH HHS R37 DK057665
6 · The paper itself

Abstract

Significantly higher levels of plasma CXCL13 [chemokine (C-X-C motif) ligand 13] were associated with the generation of broadly neutralizing antibodies (bnAbs) against HIV in a large longitudinal cohort of HIV-infected individuals. Germinal centers (GCs) perform the remarkable task of optimizing B-cell Ab responses. GCs are required for almost all B-cell receptor affinity maturation and will be a critical parameter to monitor if HIV bnAbs are to be induced by vaccination. However, lymphoid tissue is rarely available from immunized humans, making the monitoring of GC activity by direct assessment of GC B cells and germinal center CD4(+) T follicular helper (GC Tfh) cells problematic. The CXCL13-CXCR5 [chemokine (C-X-C motif) receptor 5] chemokine axis plays a central role in organizing both B-cell follicles and GCs. Because GC Tfh cells can produce CXCL13, we explored the potential use of CXCL13 as a blood biomarker to indicate GC activity. In a series of studies, we found that plasma CXCL13 levels correlated with GC activity in draining lymph nodes of immunized mice, immunized macaques, and HIV-infected humans. Furthermore, plasma CXCL13 levels in immunized humans correlated with the magnitude of Ab responses and the frequency of ICOS(+) (inducible T-cell costimulator) Tfh-like cells in blood. Together, these findings support the potential use of CXCL13 as a plasma biomarker of GC activity in human vaccine trials and other clinical settings.

Indexed as

AnimalsBiomarkersChemokine CXCL13Cohort StudiesEnzyme-Linked Immunosorbent AssayFlow CytometryGerminal CenterHIV InfectionsHumansLymph NodesMacacaMice, Inbred C57BLVaccinationBiomarkersChemokine CXCL13antibodiesCXCL13HIVTfhvaccines

Identifiers

PMID26908875
PMCPMC4790995
OpenAlexW2286883753

What OpenQuestion holds

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Registered trials

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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.