Evidence map›Paper›PMID 7769101›Full record

ArticleThe Journal of clinical investigation1995

Adoptive transfer of lymphocytes sensitized to the major surface glycoprotein of Pneumocystis carinii confers protection in the rat.

S A Theus, R P Andrews, P Steele, P D Walzer

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

22 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Seroepidemiological study of Pneumocystis jirovecii infection in healthy infants in Chile using recombinant fragments of the P. jirovecii major surface glycoprotein.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2010
    Article
  5. Geographical variation in serological responses to recombinant Pneumocystis jirovecii major surface glycoprotein antigens.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2009
    Article
  6. Article
  7. Article
  8. Article
  9. A novel approach to restore lung immunity during systemic immunosuppression.Transactions of the American Clinical and Climatological Association · 2005
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Immunological features of Pneumocystis carinii infection in humans.Clinical and diagnostic laboratory immunology · 1999
    Review
  16. Article
  17. Article
  18. Article
  19. Prospects for the development of fungal vaccines.Clinical microbiology reviews · 1997
    Review
  20. 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

4 authors at 2 institutions in 1 country.

S A TheusResearch Service, Veterans Affairs Medical Center, Cincinnati, OH 45220, USA.
R P Andrews
P Steele
P D Walzer
University of Cincinnati Medical Center · USVeterans Health Administration · US

Funding

CONTROL OF TYPE II CELL FUNCTION BY PNEUMOCYSTIS CARINIIR01HL046653 · NHLBI · UNIVERSITY OF CINCINNATI · PI RICE, WARD R · 1991 to 1994
–
PURINE METABOLISM IN TOXOPLASMA GONDII AND PNEUMOCYSTIS CARINIIU01AI031702 · NIAID · UNIVERSITY OF CINCINNATI · PI KALB, VERNON F · 1991 to 1993
–
NHLBI NIH HHS HL-46653NIAID NIH HHS AI-25139NIAID NIH HHS AI31702
6 · The paper itself

Abstract

Pneumocystis carinii is a major opportunistic pathogen and a leading cause of morbidity in patients with AIDS. CD4+ cells have been shown to be important in host defenses against P. carinii, but the antigen(s) involved with this response have not been identified. We undertook the present study to determine whether the major surface glycoprotein (MSG) of P. carinii contains epitopes that can elicit a protective cellular immune response. Spleen cells and purified CD4+ cells isolated from Lewis rats, pulsed 1-4 d with MSG, and injected into corticosteroid-treated Lewis rats with pneumocystosis resulted in significant reduction in the P. carinii burden, as judged by organism quantitation and lung histology. The protective response demonstrated by the donor cells was dependent on previous exposure to P. carinii, cell concentration, and time of incubation with MSG. In addition, reconstitution with MSG-specific CD4+ cells resulted in an early hyperinflammatory response within the lungs of these animals with a high percentage of mortality. Thus, in this model, MSG can elicit an immune response mediated by CD4+ cells, which has a harmful as well as helpful effect on the host, and these responses occur despite the presence of corticosteroids.

Indexed as

AnimalsAntigens, FungalFungal ProteinsImmunity, CellularImmunization, PassiveImmunosuppression TherapyMaleMembrane GlycoproteinsPneumocystisPneumonia, PneumocystisRatsRats, Inbred LewT-Lymphocyte SubsetsAntigens, FungalFungal ProteinsGPA protein, Pneumocystis carinii sp.Membrane Glycoproteins

Identifiers

PMID7769101
PMCPMC295941
OpenAlexW2014022546

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.