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Pharma Investments, Ventures & Law Weekly



March 12, 2006 EXPANDED REPORTING; Pg. 108





IOWA STATE UNIVERSITY

Study investigated porcine reproductive and respiratory syndrome virus

vaccine



Investigators evaluate immune responses and protection by vaccine and various

vaccine adjuvant candidates to virulent porcine reproductive and respiratory

syndrome virus in a recent issue of Veterinary Immunology and

Immunopathology.



"Various vaccine adjuvant candidates were assessed with the modified-live porcine

reproductive and respiratory syndrome virus (MLV PRRSV) (Ingelvac PRRS MLV)

vaccine. Their influence on humoral-mediated immune (HMI) and cell-mediated immune

(CMI) responses as well as protection from virulent PRRSV challenge (MN-184) was

evaluated," researchers in the United States report.



Wasin Charerntantankul and collaborators at Iowa State University and Boehringer

Ingelheim Vetmedica, Inc. wrote, "Ninety seronegative pigs were randomly divided into

nine groups of 10 pigs. One group received MLV vaccine alone. Five groups received

MLV vaccine with either bacterial endotoxin-derived adjuvant (ET), mixed open reading

frame 5 (ORF5) peptides derived from various PRRSV isolates, porcine interferon alpha

(IFN alpha), polyinosinic-polycytidylic acid stabilized with polylysine and carboxymethyl

cellulose (poly-ICLC), or porcine interleukin-12 (IL-12). One group did not receive MLV

vaccine but was immunized with ORF5 peptides conjugated with cholera toxin (ORF5

peptide/CT). Two groups served as challenged and unchallenged nonvaccinated

controls."



Charerntantankul and associates stated, "Four-color flow cytometry was utilized to

simultaneously identify three major porcine T-cell surface markers (CD4, CD8, and

gamma delta TCR) and detect activation marker CD25 (alpha chain of IL-2 receptor) or

intracellular IFN-gamma. The MLV PRRSV vaccine alone successfully primed CD4-

CD8+gamma delta- T-cells as demonstrated by a significant increase in %IFN-gamma+

cells when live PRRSV was used as a recall antigen."



"Booster immunizations of mixed ORF5 peptides and co-administration of IL-12 with

MLV PRRSV vaccine significantly enhanced IFN-gamma expression by some T-cell

subsets (CD4-CD8+gamma delta+ and CD4-CD8-gamma delta+ for mixed ORF5

peptides and CD4+CD8+gamma delta- and CD4-CD8+gamma delta+ for IL-12),"

reported the scientists. "All groups receiving MLV-vaccine with or without adjuvants had

reduced lung lesions after challenge. The group immunized with only ORF5 peptide/CT

did not have significant T-cell recall responses and was not protected from challenge."



"Expression of IFN-gamma by several T-cell subsets correlated with reduced lung

lesions and viremia, whereas expression of CD25 did not," noted the investigators.

"Expression of surface CD25 did not correlate with IFN-gamma production. PRRSV

ELISA s/p ratio prior to challenge also correlated with reduced lung lesions and viremia.

Booster immunizations of the mixed ORF5 peptides and co-administration of IL-12

effectively enhanced the CMI response to MLV vaccine. However, neither adjuvant

significantly contributed to reducing clinical effects when compared to MLV alone."



Charerntantankul and coauthors published their study in Veterinary Immunology and

Immunopathology (Immune responses and protection by vaccine and various vaccine

adjuvant candidates to virulent porcine reproductive and respiratory syndrome virus. Vet

Immunol Immunopathol, 2006;109(1-2):99-115).



For additional information, contact James A. Roth, Department of Veterinary

Microbiology and Preventive Medicine, Iowa State University, College of Veterinary

Medicine, Ames, IA 50011-1250, USA. E-mail: jaroth@iastate.edu.



The publisher of the journal Veterinary Immunology and Immunopathology can be

contacted at: Elsevier Science BV, PO Box 211, 1000 AE Amsterdam, The Netherlands.



Keywords: Ames, Iowa, United States, Virology Vaccine, Vaccine Development, Vaccine

Adjuvant, Vaccine Efficacy, Porcine Reproductive and Respiratory Syndrome Virus,

Immunology, Immunotherapy, Proteomics, Veterinary Medicine.



This article was prepared by Pharma Investments, Ventures & Law Weekly editors from

staff and other reports.



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