Evidence map›Paper›PMID 11349041›Full record

ArticleInfection and immunity2001

Functional activity of anti-Neisserial surface protein A monoclonal antibodies against strains of Neisseria meningitidis serogroup B.

G R Moe, P Zuno-Mitchell, S S Lee, A H Lucas, D M Granoff

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 48 citations in OpenAlex.

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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.

G R MoeChildren's Hospital Oakland Research Institute, California 94609, USA.
P Zuno-Mitchell
S S Lee
A H Lucas
D M Granoff

Funding

ZIDOVUDINE &LAMIVUDINE &NEVIRAPINE COMBINATION THERAPY IN HIV 1 INFM01RR001271 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KESSLER, DAVID A · 1985 to 2006
$22.7M
Novel vaccine strategies for prevention of N. meningitidis group B diseaseR01AI046464 · NIAID · OMVAX, INC. · PI MOE, GREGORY ROBERT · 2000 to 2024
$12.1M
MIMETICS OF CAPSULAR EPITOPES OF NEISSERIA MENINGITIDISR01AI045642 · NIAID · CHILDREN'S HOSPITAL &RES CTR AT OAKLAND · PI MOE, GREGORY R · 2000 to 2004
$2.9M
HUMAN ANTIBODY REPERTOIRE TO H INFLUENZAE BR37AI025008 · NIAID · CHILDREN'S HOSPITAL &RES CTR AT OAKLAND · PI LUCAS, ALEXANDER H. · 1995 to 2004
$2.5M
Polysaccharide Antibody RepertoiresR01AI025008 · NIAID · SCRIPPS CLINIC AND RESEARCH FOUNDATION · PI LUCAS, ALEXANDER H. · 1987 to 2010
$2.0M
NCRR NIH HHS M01 RR001271NCRR NIH HHS RR01271NIAID NIH HHS AI25008NIAID NIH HHS AI46464NIAID NIH HHS R01 AI025008NIAID NIH HHS R01 AI045642NIAID NIH HHS R01 AI046464NIAID NIH HHS R01 AI45642NIAID NIH HHS R37 AI025008
6 · The paper itself

Abstract

Neisserial surface protein A (NspA) is currently being investigated with humans as a candidate vaccine for the prevention of meningococcal disease. Although NspA is highly conserved, the ability of anti-NspA antibodies to bind to or elicit complement-mediated bactericidal activity against diverse Neisseria meningitidis serogroup B strains is controversial. To evaluate strain differences in NspA surface accessibility and susceptibility to bactericidal activity, we prepared murine immunoglobulin G2a anti-NspA monoclonal antibodies (MAbs) and evaluated their functional activity against 10 genetically diverse N. meningitidis serogroup B strains. By colony Western blot, all 10 strains expressed NspA as detected by one or more MAbs. By flow cytometry, two MAbs were found to bind to the bacterial surface of 6 of the 10 strains. In addition, two strains showed variable NspA surface accessibility for the MAbs despite being uniformly positive for NspA expression by colony Western blotting. Only 4 of the 10 strains were susceptible to anti-NspA complement-mediated bacteriolysis. Passively administered MAb protected infant rats from developing bacteremia after challenge with N. meningitidis serogroup B strain 8047 (surface binding positive, susceptible to anti-NspA bacteriolysis), was poorly protective against strain BZ232 (surface binding variable, resistant to bacteriolysis), and did not protect against strain M986 (surface binding negative, resistant to bacteriolysis). Finally, NspA does not appear to be critical for causing bacteremia, as an NspA knockout from strain 8047 was highly virulent in infant rats. Taken together, these findings suggest that an NspA-based vaccine will need to incorporate additional antigens to elicit broad protection against N. meningitidis serogroup B.

Indexed as

AnimalsAntibodies, BacterialAntibodies, MonoclonalAntigens, BacterialBacteremiaBacterial Outer Membrane ProteinsBacterial VaccinesBacteriolysisFemaleHumansImmune SeraMeningococcal InfectionsMiceNeisseria meningitidisRatsRats, WistarAntibodies, BacterialAntibodies, MonoclonalAntigens, BacterialBacterial Outer Membrane ProteinsBacterial VaccinesImmune SeraNspA protein, Neisseria

Identifiers

PMID11349041
PMCPMC98387
OpenAlexW2127194736

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.