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C5a peptidase enhances clearance of group B Strep from lungs of infected mice.

Vaccine Weekly

| January 01, 2003 | COPYRIGHT 2003 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2003 JAN 1 - (NewsRx.com & NewsRx.net) -- According to a study from the United States, "Group B streptococci (GBS) are among the most common causes of life-threatening neonatal infections. Vaccine development since the late 1970s has focused on the capsular polysaccharides, but a safe, effective product is still not available."

Q. Cheng and colleagues, University of Minnesota, said their "quest for a vaccine turned to the streptococcal C5a peptidase (SCPB). This surface protein is antigenically conserved across most if not all serotypes," they noted.

They used a mouse model "to assess the impact of SCPB on clearance of GBS from the lungs of intranasally infected animals."

The researchers reported that "[m]utational inactivation of SCPB resulted in more-rapid clearance of streptococci from the lung."

"Immunization with recombinant SCPB alone or SCPB conjugated to type III capsular polysaccharide produced serotype-independent protection, which was evidenced by more-rapid clearance of the serotype VI strain from the lungs," they wrote.

"Immunization of mice with tetanus toxoid-type III polysaccharide conjugate did not produce protection, confirming that protection induced by SCPB conjugates was independent of type III polysaccharide antigen. Histological ...

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Source: HighBeam Research, C5a peptidase enhances clearance of group B Strep from lungs of...

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