Evidence map›Paper›PMID 23913680›Full record

ArticlePathogens and disease2014

Interaction of Cryptosporidium parvum with mouse dendritic cells leads to their activation and parasite transportation to mesenteric lymph nodes.

Gregorio Perez-Cordon, Guilin Yang, Boping Zhou, Weijia Nie, Shan Li, Lianfa Shi, Saul Tzipori, Hanping Feng

Open access · bronzeAbstract read
In one paragraph

Article in Pathogens and disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

13 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Frontiers in immunology · 2024
    Article
  6. Dendritic Cells andMicroorganisms · 2023
    Review
  7. Early immune and host cell responses toFrontiers in parasitology · 2023
    Article
  8. The Mucosal Innate Immune Response toFrontiers in cellular and infection microbiology · 2021
    Review
  9. Review
  10. Review
  11. Review
  12. Systemic and Mucosal Immune Responses toCurrent tropical medicine reports · 2015
    Article
  13. 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

8 authors at 2 institutions in 1 country.

Gregorio Perez-CordonDivision of Infectious Diseases, Department of Biomedical Sciences, Tufts University Cummings School of Veterinary Medicine, North Grafton, MA, USA.
Guilin Yang
Boping Zhou
Weijia Nie
Shan Li
Lianfa Shi
Saul Tzipori
Hanping Feng
Tufts University · USUniversity of Maryland, Baltimore · US

Funding

Development of Vaccines against Clostridium difficile InfectionR01AI088748 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI FENG, HANPING, TZIPORI, SAUL R · 2010 to 2014
$3.1M
Innate immunity and dendritic cells in cryptosporidiosisR01AI071300 · NIAID · TUFTS UNIVERSITY BOSTON · PI TZIPORI, SAUL R · 2006 to 2010
$1.8M
Epithelium, dendritic cells, and Clostridium difficile associated colitisR01DK084509 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI FENG, HANPING · 2010 to 2014
$1.7M
The role of dendritic cells in T cell immunity to CryptosporidiumK01DK076549 · NIDDK · TUFTS UNIVERSITY BOSTON · PI FENG, HANPING · 2007 to 2011
$605k
NIAID NIH HHS R01 AI071300NIAID NIH HHS R01AI071300NIAID NIH HHS R01 AI088748NIDDK NIH HHS K01 DK076549NIDDK NIH HHS K01DK076549NIDDK NIH HHS R01 DK084509NIDDK NIH HHS R01DK084509
6 · The paper itself

Abstract

Dendritic cells (DCs) are the antigen-presenting cells capable of activating naïve T cells. Although CD4+ T cells are crucial for Cryptosporidium parvum clearance, little is known about the role of DCs in the immune response to this parasite. In this study, the interaction between mouse DCs and C. parvum was investigated both in vitro and in vivo. For in vitro experiments, mouse bone marrow-derived dendritic cells (BMDCs) derived from wild-type C57B1/6 or MyD88-/- or C3H/HeJ mice and DC cell line DC2.4 were pulsed with C. parvum. Active invasion of parasites was demonstrated by parasite colocalization with host cell membranes and actin-plaque formation at the site of attachment. DC activation induced by the parasite invasion was demonstrated by upregulation of costimulatory molecules CD40, CD80, and CD86, as well as inflammatory cytokines IL-12, TNF-α, and IL-6. BMDCs derived from MyD88-/- and C3H/HeJ mice failed to produce IL-12 in response to C. parvum, suggesting the importance of TLR-dependent signaling pathway specially presence of a functional TLR4 pathway, for C. parvum-induced cytokine production. In vivo experiments showed that both parasite antigens and live parasites were transported to mice mesenteric lymph nodes. All together, these data suggest that DCs play a key role in host immune responses to C. parvum and pathogenesis of the disease.

Indexed as

AnimalsBone Marrow CellsCell LineCell MembraneCryptosporidiosisCryptosporidium parvumDendritic CellsInterleukin-12Interleukin-6Lymph NodesMiceMice, Inbred C3HMice, Inbred C57BLSignal TransductionToll-Like Receptor 4Tumor Necrosis Factor-alphaInterleukin-12Interleukin-6Tlr4 protein, mouseToll-Like Receptor 4Tumor Necrosis Factor-alphaCryptosporidium parvumdendritic cellmesenteric lymph node

Identifiers

PMID23913680
PMCPMC4426866
OpenAlexW2102803921

What OpenQuestion holds

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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.