Evidence map›Paper›PMID 9353062›Full record

ArticleInfection and immunity1997

Profiles of healing and nonhealing Cryptosporidium parvum infection in C57BL/6 mice with functional B and T lymphocytes: the extent of gamma interferon modulation determines the outcome of infection.

C M Theodos, K L Sullivan, J K Griffiths, S Tzipori

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In one paragraph

Article in Infection and immunity, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

46 citing papers in PubMed, 112 citations in OpenAlex.

  1. Article
  2. Article
  3. Interferon-Science (New York, N.Y.) · 2024
    Review
  4. Early immune and host cell responses toFrontiers in parasitology · 2023
    Article
  5. Article
  6. Article
  7. The Mucosal Innate Immune Response toFrontiers in cellular and infection microbiology · 2021
    Review
  8. Microorganisms · 2020
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Cryptosporidiosis: environmental, therapeutic, and preventive challenges.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2010
    Review
  19. Article
  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 1 institution in 1 country.

C M TheodosDepartment of Biomedical Sciences, Tufts University School of Veterinary Medicine, North Grafton, Massachusetts 01536, USA. ctheodos@opal.tufts.edu
K L Sullivan
J K Griffiths
S Tzipori
Tufts University · US

Funding

INTERFERON GAMMA AND THE IMMUNE RESPONSE TO C PARVUMR29AI039967 · NIAID · TUFTS UNIVERSITY BOSTON · PI THEODOS, CYNTHIA M · 1996 to 2000
$125k
DEVELOPMENT OF DRUGS FOR CRYPTOSPORIDIUM INFECTIONN01AI025143 · NIAID · TUFTS UNIVERSITY BOSTON · PI TZIPORI, SAUL R · 1992 to 1997
–
NIAID NIH HHS N0I-AI-25143NIAID NIH HHS R29-AI-39967
6 · The paper itself

Abstract

This study describes healing and nonhealing models of Cryptosporidium parvum infection with adult mice that have functional T and B lymphocytes. In our nonhealing model, mice on a C57BL/6 background which have a targeted disruption in the gamma interferon (IFN-gamma) gene (GKO mice) are utilized. C. parvum-infected GKO mice shed extremely high levels of oocysts and displayed overwhelming infection of the entire small intestine. The majority of these mice succumbed within 2 to 3 weeks due to severe acute infection and profound mucosal destruction. In our healing murine model, C57BL/6J mice treated with a single injection of the neutralizing anti-IFN-gamma monoclonal antibody XMG 1.2 prior to infection were used. These mice developed two peaks of oocyst shedding but were ultimately free of parasites on day 30 of infection. Again, the small intestine was the primary site of infection. Mesenteric lymph node (MLN) cells isolated from C. parvum-infected nonhealing GKO mice proliferated and secreted interleukin 2 (IL-2) but not IFN-gamma or IL-4 in response to ex vivo restimulation with intact C. parvum sporozoites or a C. parvum sporozoite antigen preparation. In contrast, parasite-specific MLN cells isolated from healing C57BL/6J mice secreted IL-2 and IFN-gamma but not IL-4. These results suggest that IFN-gamma, either directly or indirectly, is important for resistance to and resolution of cryptosporidiosis. Moreover, these models now allow the analysis of parasite-specific cell-mediated and humoral mucosal immune responses to determine what constitutes protective immunity to C. parvum.

Indexed as

AnimalsAntibodies, ProtozoanB-LymphocytesBody WeightCryptosporidiosisCryptosporidium parvumInterferon-gammaLymphocyte ActivationMiceMice, Inbred C57BLRatsT-LymphocytesAntibodies, ProtozoanInterferon-gamma

Identifiers

PMID9353062
PMCPMC175683
OpenAlexW1930282251

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.