Abstract |
Two recombinant antigens which individually protect mice from lethal intranasal infection were studied in combination, either as a mixture of two separately expressed proteins or as a single chimeric expression product. Mice vaccinated with either combination survived longer than mice given single antigens. Immunized mice also exhibited specific IgG immunoglobulins and yielded splenocytes which produced interferon-gamma in response to either antigen. The chimeric antigen has the practical advantage of offering enhanced protection from multiple components without increasing production costs.
|
Authors | Lisa F Shubitz, Jieh-Juen Yu, Chiung-Yu Hung, Theo N Kirkland, Tao Peng, Robert Perrill, Julie Simons, Jianmin Xue, Roger A Herr, Garry T Cole, John N Galgiani |
Journal | Vaccine
(Vaccine)
Vol. 24
Issue 31-32
Pg. 5904-11
(Jul 26 2006)
ISSN: 0264-410X [Print] Netherlands |
PMID | 16759762
(Publication Type: Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
|
Chemical References |
- Fungal Proteins
- Fungal Vaccines
- Vaccines, Subunit
- Vaccines, Synthetic
|
Topics |
- Amino Acid Sequence
- Animals
- Coccidioides
- Coccidioidomycosis
(microbiology, prevention & control)
- Female
- Fungal Proteins
(genetics, therapeutic use)
- Fungal Vaccines
(therapeutic use)
- Mice
- Mice, Inbred C57BL
- Molecular Sequence Data
- Respiratory Tract Infections
(microbiology, prevention & control)
- Vaccines, Subunit
(therapeutic use)
- Vaccines, Synthetic
(therapeutic use)
|