Potential Zika vaccine protects against infection, pregnancy transmission and testicular damage
University of Texas Medical Branch at Galveston Oct 04, 2017
After a single dose, the developing Zika vaccine completely prevents against infection, transmission from pregnant mother to developing fetus. The vaccine also prevents damage to the male reproductive system.
For the first time, a collaborative team led by The University of Texas Medical Branch at Galveston has shown that a potential Zika vaccine quickly can protect fetuses against infection as well as protect males against testicular infection and injury. It also prevents a lowered sperm count after one vaccination.
The findings were published in the journal Nature Communications.
Although Zika infection typically results in mild or symptom-free infections in healthy individuals, infected pregnant women without symptoms may still give birth to a baby with birth defects like microcephaly. Similarly, infected men without noticeable signs of illness may still incur testicular injury and lowered sperm count. The Zika virus could infect the male reproductive system for several months, posing risk for sexual transmission.
ÂThis study showed, for the first time, that a single-dose vaccine candidate could prevent Zika infection in non-human primates, block mother-to-fetus transmission, and stop male testis infection in mice, said UTMBÂs Pei-Yong Shi, senior author and the I.H. Kempner professor at the department of biochemistry and molecular biology. ÂBesides quickly mounting a protective immune response, this live-attenuated vaccine exhibited an excellent safety profile in both mouse and non-human primate models. Taken together, the results suggest that this vaccine merits further development in humans.Â
ÂHaving a Zika vaccine that can protect male reproductive systems, pregnant women and their unborn babies would improve public health efforts to avoid birth defects and other effects of the disease in regions where Zika is circulating, said Pedro Vasconcelos, director of Evandro Chagas Institute in Brazil and co-developer of this vaccine. ÂItÂs important to note that a single-dose vaccine is practically important; vaccines that require booster shots are impractically challenging for people living in developing regions where access to medical facilities may be limited.Â
Other authors include UTMBÂs Chao Shan, Antonio Muruato, Bruno Nunes, Daniele Medeiros, Xuping Xie, Jannyce Nunes, Alan Barrett, Scott Weaver and Shannan Rossi; Justin Richner, Brett Jagger and Michael Diamond from Washington University School of Medicine; Kaitlyn Morabito, Wing-Pui Kong, Barney Graham and Theodore Pierson from the National Institutes of Health as well as Pedro Vasconcelos from Evandro Chagas Institute, Ministry of Health, Parå State University, Brazil.
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For the first time, a collaborative team led by The University of Texas Medical Branch at Galveston has shown that a potential Zika vaccine quickly can protect fetuses against infection as well as protect males against testicular infection and injury. It also prevents a lowered sperm count after one vaccination.
The findings were published in the journal Nature Communications.
Although Zika infection typically results in mild or symptom-free infections in healthy individuals, infected pregnant women without symptoms may still give birth to a baby with birth defects like microcephaly. Similarly, infected men without noticeable signs of illness may still incur testicular injury and lowered sperm count. The Zika virus could infect the male reproductive system for several months, posing risk for sexual transmission.
ÂThis study showed, for the first time, that a single-dose vaccine candidate could prevent Zika infection in non-human primates, block mother-to-fetus transmission, and stop male testis infection in mice, said UTMBÂs Pei-Yong Shi, senior author and the I.H. Kempner professor at the department of biochemistry and molecular biology. ÂBesides quickly mounting a protective immune response, this live-attenuated vaccine exhibited an excellent safety profile in both mouse and non-human primate models. Taken together, the results suggest that this vaccine merits further development in humans.Â
ÂHaving a Zika vaccine that can protect male reproductive systems, pregnant women and their unborn babies would improve public health efforts to avoid birth defects and other effects of the disease in regions where Zika is circulating, said Pedro Vasconcelos, director of Evandro Chagas Institute in Brazil and co-developer of this vaccine. ÂItÂs important to note that a single-dose vaccine is practically important; vaccines that require booster shots are impractically challenging for people living in developing regions where access to medical facilities may be limited.Â
Other authors include UTMBÂs Chao Shan, Antonio Muruato, Bruno Nunes, Daniele Medeiros, Xuping Xie, Jannyce Nunes, Alan Barrett, Scott Weaver and Shannan Rossi; Justin Richner, Brett Jagger and Michael Diamond from Washington University School of Medicine; Kaitlyn Morabito, Wing-Pui Kong, Barney Graham and Theodore Pierson from the National Institutes of Health as well as Pedro Vasconcelos from Evandro Chagas Institute, Ministry of Health, Parå State University, Brazil.
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