Evidence map›Paper›PMID 24962092›Full record

ArticleMucosal immunology2015

Antibody blocks acquisition of bacterial colonization through agglutination.

A M Roche, A L Richard, J T Rahkola, E N Janoff, J N Weiser

Abstract read
In one paragraph

Article in Mucosal immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
–field-weighted citation impact
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

74 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Bacterial and host factors affecting acquisition ofbioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. Article
  10. A Comprehensive Review of the Bovine Immune Response to Pathogens.International journal of molecular sciences · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. A Review of the Resistance Mechanisms forMedicina (Kaunas, Lithuania) · 2023
    Review
  20. Influence of glycan structure on the colonization ofProceedings of the National Academy of Sciences of the United States of America · 2023
    Article

14 more citing papers are in PubMed but not listed here.

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

5 authors.

A M RocheDepartment of Microbiology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
A L RichardDepartment of Microbiology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
J T Rahkola1] Mucosal and Vaccine Research Program Colorado (MAVRC), Division of Infectious Disease, University of Colorado Denver, Aurora, Colorado, USA [2] Denver Veterans Affairs Medical Center, Denver, Colorado, USA.
E N Janoff1] Mucosal and Vaccine Research Program Colorado (MAVRC), Division of Infectious Disease, University of Colorado Denver, Aurora, Colorado, USA [2] Denver Veterans Affairs Medical Center, Denver, Colorado, USA.
J N WeiserDepartment of Microbiology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Funding

TRANSGENIC AND CHIMERIC MOUSE COREP30DK050306 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Ken Hashigiwa Cadwell · 1997 to 2026
$32.5M
ROLE OF OPACITY VARIATION IN PNEUMOCOCCAL PATHOGENESISR01AI038446 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI WEISER, JEFFREY NEAL · 1996 to 2019
$7.4M
Mechanisms of Pneumococcal Persistence During CarriageR37AI038446 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Jeffrey Neal Weiser · 2020 to 2026
$3.8M
Mechanisms of Impaired HIV-associated B cell and Pneumococcal Vaccine responsesR01AI108479 · NIAID · UNIVERSITY OF COLORADO DENVER · PI JANOFF, EDWARD N · 2014 to 2018
$2.3M
Early Events in Pneumococcal ColonizationR01AI105168 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI WEISER, JEFFREY NEAL · 2014 to 2018
$2.1M
Cross-serotype protection against Streptococcus pneumoniae by induction of neutraR21AI092468 · NIAID · UNIVERSITY OF COLORADO DENVER · PI JANOFF, EDWARD N · 2011 to 2012
$421k
NIAID NIH HHS AI05168NIAID NIH HHS AI092468NIAID NIH HHS AI108479NIAID NIH HHS AI38446NIAID NIH HHS R01 AI038446NIAID NIH HHS R01 AI105168NIAID NIH HHS R01 AI108479NIAID NIH HHS R21 AI092468NIAID NIH HHS R37 AI038446NIDDK NIH HHS P30 DK050306NIDDK NIH HHS P30-DK050306
6 · The paper itself

Abstract

Invasive infection often begins with asymptomatic colonization of mucosal surfaces. A murine model of bacterial colonization with Streptococcus pneumoniae was used to study the mechanism for mucosal protection by immunoglobulin. In previously colonized immune mice, bacteria were rapidly sequestered within large aggregates in the nasal lumen. To further examine the role of bacterial agglutination in protection by specific antibodies, mice were passively immunized with immunoglobulin G (IgG) purified from antipneumococcal sera or pneumococcal type-specific monoclonal human IgA (hIgA1 or hIgA2). Systemically delivered IgG accessed the mucosal surface and blocked acquisition of colonization and transmission between littermates. Optimal protection by IgG was independent of Fc fragment and complement and, therefore, did not involve an opsonophagocytic mechanism. Enzymatic digestion or reduction of IgG before administration showed that protection required divalent binding that maintained its agglutinating effect. Divalent hIgA1 is cleaved by the pneumococcal member of a family of bacterial proteases that generate monovalent Fabα fragments. Thus, passive immunization with hIgA1 blocked colonization by an IgA1-protease-deficient mutant (agglutinated) but not the protease-producing wild-type parent (not agglutinated), whereas protease-resistant hIgA2 agglutinated and blocked colonization by both. Our findings highlight the importance of agglutinating antibodies in mucosal defense and reveal how successful pathogens evade this effect.

Indexed as

AgglutinationAnimalsAntibodies, MonoclonalBacterial ProteinsCell Growth ProcessesColony Count, MicrobialDisease Models, AnimalHumansImmune EvasionImmunoglobulin AImmunoglobulin GMiceMice, Inbred C57BLMutationNasal MucosaPeptide HydrolasesAntibodies, MonoclonalBacterial ProteinsImmunoglobulin AImmunoglobulin GPeptide Hydrolases

Identifiers

PMID24962092
PMCPMC4268183

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.