Evidence map›Paper›PMID 19782149›Full record

ArticleMicrobes and infection2010

Protection against nontypeable Haemophilus influenzae challenges by mucosal vaccination with a detoxified lipooligosaccharide conjugate in two chinchilla models.

Wenzhou Hong, Daxin Peng, Maritza Rivera, Xin-Xing Gu

Abstract read
In one paragraph

Article in Microbes and infection, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Journal of bacteriology · 2026
    Review
  2. Article
  3. Immunization with Protein D from Non-TypeableJundishapur journal of microbiology · 2016
    Article
  4. Article
  5. Article
  6. Article
  7. Genome sequencing of disease and carriage isolates of nontypeable Haemophilus influenzae identifies discrete population structure.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  8. Panel 6: Vaccines.Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery · 2013
    Review
  9. Article
  10. Review
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.

Wenzhou HongVaccine Research Section, National Institute on Deafness and Other Communication Disorders, Rockville, Maryland 20850, USA.
Daxin Peng
Maritza Rivera
Xin-Xing Gu
National Institutes of Health · US

Funding

VACCINE DEVELOPMENT OF NONTYPEABL HAEMOPHILUS INFLUENZAEZ01DC000019 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI GU, XIN-XING · 1994 to 2008
$1.5M
Vaccine Development Of Nontypeable Haemophilus influenzae/Moraxella catarrhalisZIADC000019 · NIDCD · NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS · PI GU, XIN-XING · 2009 to 2010
$1.3M
Intramural NIH HHS Z01 DC000019
6 · The paper itself

Abstract

Otitis media (OM) can occur following outset of upper respiratory tract infections. Inhibition of bacterial colonization in nasopharynx (NP) by mucosal vaccination may prevent OM by reducing bacterial invasion of the middle ears (MEs). In this study, 80 chinchillas were intranasally (i.n.) immunized with a detoxified lipooligosaccharide (dLOS)-tetanus toxoid conjugate vaccine of nontypeable Haemophilus influenzae (NTHi) mixed with cholera toxin (CT) or CT alone. All vaccinated animals responded with elevated levels of mucosal and serum anti-LOS antibodies. Two weeks after the last immunization, 40 chinchillas were challenged i.n. with NTHi to evaluate NP colonization and ME infection while the rest of the animals were challenged transbullarly (T.B.) to examine the development of OM. Compared to the control group, the vaccination inhibited not only bacterial colonization in NP and transmission to MEs in the i.n. challenge group but also bacterial colonization in NP and transmission to unchallenged ears in the T.B. challenge group. Though no difference was found in the challenged ears of either group right after the T.B. challenge, an early clearance of NTHi from NP and unchallenged ears as well as less severity of OM in the unchallenged ears were observed in vaccinated animals. Current results along with our previous data indicate that mucosal vaccination is capable of inhibiting NTHi NP colonization and preventing OM occurrence in chinchillas; the i.n. challenge model is preferable for testing the mucosal vaccines while the T.B. challenge model is superior for testing the systemic vaccines.

Indexed as

Adjuvants, ImmunologicAdministration, IntranasalAnimalsCarrier StateChinchillaCholera ToxinDisease Models, AnimalHaemophilus InfectionsHaemophilus influenzaeHaemophilus VaccinesHumansLipopolysaccharidesNasopharynxOtitis MediaTetanus ToxoidVaccines, ConjugateAdjuvants, ImmunologicCholera ToxinHaemophilus Vaccineslipid-linked oligosaccharidesLipopolysaccharidesTetanus ToxoidVaccines, Conjugate

Identifiers

PMID19782149
PMCPMC2818210
OpenAlexW2095195849

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.