Cited by 49HIV Research and TreatmentT-cell and B-cell ImmunologyHIV-related health complications and treatments

De novo T-cell generation in patients at different ages and stages of HIV-1 disease

Open access
Nobile, M.·2004·Blood

Abstract

We assessed de novo T-cell generation by determining T-cell receptor-rearrangement excision circles (TRECs) based on patient age and on stage of HIV-1 infection. TRECs were measured in purified CD4 and CD8 T cells of a large cohort of HIV-1-infected subjects (n = 297) with chronic infection but no previous antiretroviral treatment and of a control group of HIV-negative subjects (n = 120). HIV-1-infected subjects were stratified on the basis of CD4 T-cell counts in 3 groups, early-stage disease (more than 500 CD4 T cells), intermediate-stage disease (200-500 CD4 T cells), and late-stage disease (fewer than 200 CD4 T cells). Compared with the control group, CD8 TREC contents were severely reduced (P <.001) in HIV-1-infected subjects regardless of the stage of HIV disease. In contrast, CD4 TREC contents were significantly increased (P =.003) in HIV-1-infected subjects during early-stage disease, similar at intermediate-stage disease, and severely reduced only at late-stage disease. We show that the increase in CD4 TRECs was mostly limited to younger (younger than 45 years) patients at early-stage disease. Our results demonstrate a dichotomy between TREC contents in CD4 and CD8 T-cell populations in HIV-1 infection and indicate that thymus function in younger subjects is preserved at early and intermediate stages of HIV infection.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1182/blood-2003-12-4265

Cites

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • In young adults the thymus contributes only 16% of total T cell generation, and in older individuals thymic contribution falls below 1%, so they rely almost entirely on peripheral proliferation.

    “Even in young adults, the thymus contributes only 16% of total T cell generation. Thymic contribution declines further to <1% in older individuals who therefore nearly exclusively rely on peripheral proliferation to repopulate T cells”

    From Successful and Maladaptive T Cell Aging (2017) · cites this paper as Nobile et al., 2004

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

The citation lists haven’t been fetched yet

References 41 · Cited by 49

Authors
Nobile, M.
Affiliations
Centre Hospitalier Universitaire Vaudois (CH)
Corresponding author
Nobile, M.
Venue
Blood
Published
2004-07-15
Volume
104
Issue
2
Pages
470-477
ISSN
  • 0006-4971 (ISSN-L)
  • 1528-0020
OpenAlex
W2130959108
Cited by
49
References
41
Citations by year
2021: 1 · 2019: 2 · 2018: 2 · 2017: 1 · 2016: 1 · 2014: 1 · 2013: 2 · 2012: 1
FWCI
2.51
Type
journal article
Language
en
Open access
Locations
  • Blood (publishedVersion)
  • PubMed (publishedVersion)
  • Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
  • IRIS (submittedVersion)
  • SERVAL (Université de Lausanne) (submittedVersion)
Topics
  • Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Health Sciences › Medicine › Emergency Medicine › HIV-related health complications and treatments
Keywords
HIV-1 infection, CD4+ T cells, CD8+ T cells, thymic function, age differences, disease stage, CD4 count, immune reconstitution
MeSH terms
Adult, Aging, Cell Division, Humans, Middle Aged, Thymus Gland, Gene Rearrangement, T-Lymphocyte, CD4-Positive T-Lymphocytes, HIV-1, HIV Infections, Cell Death, CD8-Positive T-Lymphocytes, CD4 Lymphocyte Count, Viral Load

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review