Evidence map›Paper›PMID 8676077›Full record

ArticleThe Journal of experimental medicine1996

Interleukin-12 primes human CD4 and CD8 T cell clones for high production of both interferon-gamma and interleukin-10.

F Gerosa, C Paganin, D Peritt, F Paiola, M T Scupoli, M Aste-Amezaga, I Frank, G Trinchieri

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of experimental medicine, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
11.1field-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

89 citing papers in PubMed, 307 citations in OpenAlex.

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  11. Impact of polyphenols in phagocyte functions.Journal of inflammation research · 2019
    Article
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  17. Review
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  20. CD4+ T Cells: guardians of the phagosome.Clinical microbiology reviews · 2014
    Review

29 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

8 authors at 1 institution in 1 country.

F GerosaImmunology and Infectious Disease Institute, University of Verona, Italy.
C Paganin
D Peritt
F Paiola
M T Scupoli
M Aste-Amezaga
I Frank
G Trinchieri
University of Verona · IT

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Maureen E. Murphy · 1985 to 2026
$75.9M
CELL-MEDIATED CYTOTOXICITY IN HUMANSR01CA020833 · NCI · WISTAR INSTITUTE · PI KAUFMAN, RUSSEL E. · 1985 to 2003
$1.9M
DIFFERENTIATION AND FUNCTION OF MONOCYTESR01CA032898 · NCI · WISTAR INSTITUTE · PI SANTOLI, DANIELA · 1985 to 1994
–
CELL-MEDIATED CYTOTOXICITY IN HUMANSR37CA020833 · NCI · WISTAR INSTITUTE · PI TRINCHIERI, GIORGIO · 1990 to 1998
–
NCI NIH HHS CA10815NCI NIH HHS CA20833NCI NIH HHS CA32898
6 · The paper itself

Abstract

Interleukin-12 (IL-12) induces differentiation of T helper 1 (Th1) cells, primarily through its ability to prime T cells for high interferon-gamma (IFN-gamma) production. We now report that the presence of IL-12 during the first several days of in vitro clonal expansion in limiting dilution cultures of polyclonally stimulated human peripheral blood CD4+ and CD8+ T cells also induces stable priming for high IL-10 production. This effect was demonstrated with T cells from both healthy donors and HIV+ patients. Priming for IL-4 production, which requires IL-4, was maximum in cultures containing both IL-12 and IL-4. IL-4 modestly inhibited the IL-12-induced priming for IFN-gamma, but almost completely suppressed the priming for IL-10 production. A proportion of the clones generated from memory CD45RO+ cells, but not those generated from naive CD45RO- CD4+ T cells, produced some combinations of IFN-gamma, IL-10, and IL-4 even in the absence of IL-12 and IL-4, suggesting in vivo cytokine priming; virtually all CD4+ clones generated from either CD45RO(-) or (+) cells, however, produced high levels of both IFN-gamma and IL-10 when IL-12 was present during expansion. These results indicate that each Th1-type (IFN-gamma) and Th2-type (IL-4 and IL-10) cytokine gene is independently regulated in human T cells and that the dichotomy between T cells with the cytokine production pattern of Th1 and Th2 cells is not due to a direct differentiation-inducing effect of immunoregulatory cytokines, but rather to secondary selective mechanisms. Particular combinations of cytokines induce a predominant generation of T cell clones with anomalous patterns of cytokine production (e.g., IFN-gamma and IL-4 or IFN-gamma and IL-10) that can also be found in a proportion of fresh peripheral blood T cells with "memory" phenotype or clones generated from them and that may identify novel Th subsets with immunoregulatory functions.

Indexed as

Antigens, CDCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell DifferentiationClone CellsHIV SeropositivityHumansImmunologic MemoryImmunophenotypingInterferon-gammaInterleukin-10Interleukin-12Interleukin-4Leukocyte Common AntigensRecombinant ProteinsReference ValuesAntigens, CDInterferon-gammaInterleukin-10Interleukin-12Interleukin-4Leukocyte Common AntigensRecombinant Proteins

Identifiers

PMID8676077
PMCPMC2192598
OpenAlexW2116723397

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.