Evidence map›Paper›PMID 19949093›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

Anti-CD3 antibody decreases inflammation and improves outcome in a murine model of Pneumocystis pneumonia.

Samir P Bhagwat, Terry W Wright, Francis Gigliotti

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. T-cell subsets inClinical & translational immunology · 2025
    Review
  2. Article
  3. Immune Response inJournal of fungi (Basel, Switzerland) · 2021
    Review
  4. Article
  5. Immune reconstitution inflammatory syndrome associated withThe Journal of international medical research · 2020
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Immune Modulation as Adjunctive Therapy for Pneumocystis pneumonia.Interdisciplinary perspectives on infectious diseases · 2011
    Article
  15. 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

3 authors at 2 institutions in 1 country.

Samir P BhagwatDepartment of Pediatrics, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.
Terry W Wright
Francis Gigliotti
University of Rochester · USPediatrics and Genetics · US

Funding

P. carinii Pneumonia Lung Damage: CD8-driven Cellular and Molecular EventsR01HL092797 · NHLBI · UNIVERSITY OF ROCHESTER · PI GIGLIOTTI, FRANCIS, WRIGHT, TERRY W · 2008 to 2012
$2.0M
Chemokine regulation of immune cell recruitment during Pneumocystis pneumoniaR01HL083761 · NHLBI · UNIVERSITY OF ROCHESTER · PI WRIGHT, TERRY W · 2006 to 2010
$2.0M
NHLBI NIH HHS 1R01HL092797NHLBI NIH HHS R01 HL083761NHLBI NIH HHS R01 HL092797
6 · The paper itself

Abstract

The T cell-mediated immune response elicited by Pneumocystis plays a key role in pulmonary damage and dysfunction during Pneumocystis carinii pneumonia (PcP). Mice depleted of CD4(+) and CD8(+) T cells prior to infection are markedly protected from PcP-related respiratory deficit and death, despite progressive lung infection. However, the therapeutic effectiveness of Ab-mediated disruption of T cell function in mice already displaying clinical symptoms of disease has not been determined. Therefore, a murine model of PcP-related immune reconstitution inflammatory syndrome was used to assess whether Ab to the pan-T cell molecule CD3 is effective for reducing the severity of PcP when administered after the onset of disease. Mice that received anti-CD3 Ab exhibited a rapid and dramatic halt in the PcP-associated pulmonary function decline within 1 week after treatment, and a striking enhancement of survival rate compared with mice receiving the control Ab. Physiologic improvement in anti-CD3 treated mice was associated with a significant reduction in the number of CD4(+) and CD8(+) T cells recovered in lung lavage fluid. This effectiveness of anti-CD3 was noted whether the mice also received antibiotic therapy with trimethoprim-sulfamethoxazole. These data suggest that monoclonal Ab-mediated disruption of T cell function may represent a specific and effective adjunctive therapy to rapidly reverse the ongoing pathologic immune response occurring during active PcP. Thus, the anti-human CD3 monoclonal Ab OKT3, which is already in clinical use, has the potential to be developed as an adjunctive therapy for PcP.

Indexed as

AnimalsAntibodiesAnti-Infective AgentsBronchoalveolar Lavage FluidCD3 ComplexDisease Models, AnimalInflammationLymphocyte DepletionMicePneumonia, PneumocystisReverse Transcriptase Polymerase Chain ReactionTrimethoprim, Sulfamethoxazole Drug CombinationAntibodiesAnti-Infective AgentsCD3 ComplexTrimethoprim, Sulfamethoxazole Drug Combination

Identifiers

PMID19949093
PMCPMC2797573
OpenAlexW1711573635

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.