Recommend Human Vaccines to your librarian for 2008. Download form here.

Sign up for TOC Alerts

home subscribe search archive forthcoming

Email this page Print this page

Research Paper

A Clinical Study to Assess the Safety and Immunogenicity of Attenuated Measles Vaccine Administered Intranasally to Healthy Adults

Jakub K. Simon, Marcela F. Pasetti, Jean-François Viret, Robert Mischler, Alma Munoz, Rosanna Lagos, Myron M. Levine and James D. Campbell

volume 3 | issue 2

march/april 2007
Pages: 54 - 58

This is an open-access article

 Download PDF

If the document does not open, please right-click on the link (control-click on a Macintosh) and select the option to save the file to disk.

Background: Despite the availability of a safe and effective vaccine for over four decades, measles remains one of the most common infectious disease killers of children in the world. Mucosal administration of currently licensed measles vaccine has been proposed to address issues of needle safety and improve vaccine uptake.
Methods: Healthy adult volunteers were randomized to receive live-attenuated monovalent measles virus vaccine (Moraten Berna) via the standard subcutaneous (SQ) or the experimental intranasal (IN) route in a randomized, double-masked fashion. Safety, reactogenicity, immunogenicity, and shedding were assessed.
Results: Safety, reactogenicity, and viral shedding were not significantly different in the two study groups. Immunogenicity was markedly lower in the group of volunteers that received vaccine via the IN route. Plaque reduction neutralization (PRN) geometric mean titers (GMT) were 125 (95% confidence interval [CI] 68-228) milli International Units per milliliter (mIU/mL) on day 28 in recipients of IN vaccine versus 645 (95% CI 468-889) mIU/mL in recipients of vaccine SQ; p<0.001 by Mann-Whitney Rank Sum. 50 % of measles non-immune individuals mounted titers above the protective threshold of PRN 200 mIU/mL after IN administration versus 100% of volunteers who received the vaccine SQ.
Conclusion: Intranasal administration of live-attenuated measles vaccine was safe and well tolerated, but failed to mount significant immune responses when compared to subcutaneous administration. It is possible that higher doses or smaller particle size are necessary for successful intranasal measles vaccination and boosting.

Authors

Jakub K. Simon

Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD USA

Marcela F. Pasetti

Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD USA

Jean-François Viret

Berna Biotech Ltd., Bern, Switzerland

Robert Mischler

Berna Biotech Ltd.; Bern, Switzerland

Alma Munoz

Center for Vaccine Development, Hospital Roberto del Rio, Santiago, Chile

Rosanna Lagos

3Center for Vaccine Development, Hospital Roberto del Rio, Santiago, Chile

Myron M. Levine

Center for Vaccine Development, University of Maryland School of Medicin; Baltimore, Maryland USA

James D. Campbell

Center for Vaccine Development, University of Maryland School of Medicine; Baltimore, MD USA


This is an open-access article

 Download PDF

If the document does not open, please right-click on the link (control-click on a Macintosh) and select the option to save the file to disk.