Evidence map›Paper›PMID 18806124›Full record

ArticleJournal of leukocyte biology2008

Immune activation and IL-12 production during acute/early HIV infection in the absence and presence of highly active, antiretroviral therapy.

Adriana A Byrnes, David M Harris, Sowsan F Atabani, Beulah P Sabundayo, Susan J Langan, Joseph B Margolick, Christopher L Karp

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of leukocyte biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

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  11. Transformative tools for tackling tuberculosis.The Journal of experimental medicine · 2015
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  19. Innate and adaptive factors regulating human immunodeficiency virus type 1 genomic activation.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2010
    Review
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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

7 authors at 3 institutions in 1 country.

Adriana A ByrnesDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
David M Harris
Sowsan F Atabani
Beulah P Sabundayo
Susan J Langan
Joseph B Margolick
Christopher L Karp
Johns Hopkins University · USCincinnati Children's Hospital Medical Center · USJohns Hopkins Medicine · US

Funding

Aedes antiviral RNAi pathwayR01AI141532 · NIAID · JOHNS HOPKINS UNIVERSITY · PI George Dimopoulos, KEVIN M MYLES · 2019 to 2026
$4.6M
MOLECULAR MECHANISMS OF HIV INDUCED IMMUNOSUPPRESSIONR01DE012167 · NIDCR · JOHNS HOPKINS UNIVERSITY · PI KARP, CHRISTOPHER L · 1996 to 1998
–
NIAID NIH HHS R01 AI141532NIAID NIH HHS U01AI141532NIDCR NIH HHS R01DE12167
6 · The paper itself

Abstract

Suppressed IL-12 production and maladaptive immune activation, both of which are ameliorated by successful highly active antiretroviral therapy (HAART), are thought to play important roles in the immunopathogenesis of chronic HIV infection. Despite the important effects of the immunological and virological events of early HIV infection on subsequent disease progression, IL-12 production and immune activation in early infection remain under-defined. To quantify IL-12 production and immune activation during acute/early HIV infection, in the presence and absence of HAART, we performed a prospective, longitudinal study of participants in the Baltimore site of the Acute Infection and Early Disease Research Program, with cross-sectional comparison to healthy control subjects. PBMC cytokine productive capacity and plasma immune activation markers [soluble CD8 (sCD8), sCD4, granzyme B, neopterin, beta2-microglobulin, sIL-2R, sTNFRI, sTNFRII, and IL-12p70] were quantified by ELISA. Notably, PBMC from patients with acute/early HIV infection exhibited in vivo IL-12p70 production along with increased, maximal in vitro IL-12 production. Further, despite evidence from plasma markers of generalized immune activation, no elevation in plasma levels of sCD4 was observed, suggesting relative blunting of in vivo CD4+ T cell activation from the beginning of HIV infection. Finally, despite successful virological responses to HAART, heightened in vivo CD8+ T cell activation, IL-12 production, and IFN activity were sustained for at least 6 months during primary HIV infection. These data underscore the need for comparative mechanistic analysis of the immunobiology of early and chronic HIV infection.

Indexed as

Antiretroviral Therapy, Highly ActiveAcute DiseaseAdultBaltimoreCase-Control StudiesCD4 Lymphocyte CountCD4-Positive T-LymphocytesCytokinesEnzyme-Linked Immunosorbent AssayFemaleHIV-1HIV InfectionsHumansInterferon-gammaInterleukin-12Longitudinal StudiesCytokinesInterferon-gammaInterleukin-12RNA, Viral

Identifiers

PMID18806124
PMCPMC2614601
OpenAlexW2108189847

What OpenQuestion holds

Textmetadata
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.