Administration of antibody to the lung protects mice against pneumonic plague.
about
Antibodies for biodefenseDirect neutralization of type III effector translocation by the variable region of a monoclonal antibody to Yersinia pestis LcrVEfficacy of primate humoral passive transfer in a murine model of pneumonic plague is mouse strain-dependent.Biosafety level 2 model of pneumonic plague and protection studies with F1 and Psa.TNFα and IFNγ contribute to F1/LcrV-targeted immune defense in mouse models of fully virulent pneumonic plague.Enhancement of immune response to an antigen delivered by vaccinia virus by displaying the antigen on the surface of intracellular mature virion.Intranasal administration of an inactivated Yersinia pestis vaccine with interleukin-12 generates protective immunity against pneumonic plagueInduction of pulmonary mucosal immune responses with a protein vaccine targeted to the DEC-205/CD205 receptorRecombinant Bivalent Fusion Protein rVE Induces CD4+ and CD8+ T-Cell Mediated Memory Immune Response for Protection Against Yersinia enterocolitica Infection.Effective plague vaccination via oral delivery of plant cells expressing F1-V antigens in chloroplasts.FGL chaperone-assembled fimbrial polyadhesins: anti-immune armament of Gram-negative bacterial pathogens.Intranasal prophylaxis with CpG oligodeoxynucleotide can protect against Yersinia pestis infection.Vaccination of mice with a Yop translocon complex elicits antibodies that are protective against infection with F1- Yersinia pestisAdenovirus-mediated delivery of an anti-V antigen monoclonal antibody protects mice against a lethal Yersinia pestis challenge.D27-pLpxL, an avirulent strain of Yersinia pestis, primes T cells that protect against pneumonic plague.Adhesive organelles of Gram-negative pathogens assembled with the classical chaperone/usher machinery: structure and function from a clinical standpoint.Assessing the risk to health care staff from long-term exposure to anticancer drugs--the case of monoclonal antibodies.Affinity maturation of an anti-V antigen IgG expressed in situ through adenovirus gene delivery confers enhanced protection against Yersinia pestis challenge.Yersinia pestis can bypass protective antibodies to LcrV and activation with gamma interferon to survive and induce apoptosis in murine macrophagesAntibodies and cytokines independently protect against pneumonic plague.
P2860
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P2860
Administration of antibody to the lung protects mice against pneumonic plague.
description
2006 nî lūn-bûn
@nan
2006 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Administration of antibody to the lung protects mice against pneumonic plague.
@ast
Administration of antibody to the lung protects mice against pneumonic plague.
@en
Administration of antibody to the lung protects mice against pneumonic plague.
@nl
type
label
Administration of antibody to the lung protects mice against pneumonic plague.
@ast
Administration of antibody to the lung protects mice against pneumonic plague.
@en
Administration of antibody to the lung protects mice against pneumonic plague.
@nl
prefLabel
Administration of antibody to the lung protects mice against pneumonic plague.
@ast
Administration of antibody to the lung protects mice against pneumonic plague.
@en
Administration of antibody to the lung protects mice against pneumonic plague.
@nl
P2093
P2860
P1476
Administration of antibody to the lung protects mice against pneumonic plague
@en
P2093
Jim E Eyles
Roman A Lukaszewski
Stephen J Elvin
P2860
P304
P356
10.1128/IAI.74.5.3068-3070.2006
P407
P577
2006-05-01T00:00:00Z