The study could offer hope to others with severely compromised immune systems

DUKE UNIVERSITY MEDICAL CENTER

DURHAM, N.C. – A newer form of shingles vaccine reduced outbreaks of the painful rash among patients who were transplanted with their own stem cells, according to a study led by a Duke Health researcher and published today in JAMA. 

The vaccine appears to offer protection from one of the most common and painful side effects of cell therapy and shows promise for patients with immune-compromising conditions.

Using a non-live form of the herpes zoster virus that causes shingles, the researchers tested vaccination among people whose immune systems are wiped out during hematopoietic stem cell transplantation (HSCT). HSCT patients are especially prone to bouts of shingles, which is caused by reactivation of the latent varicella-zoster virus that also causes chicken pox. 

The outbreak results in red, painful, burning blisters and rash, typically on one side of the body and often occurs in older adults or people with weakened immune systems. In some cases, shingles causes excruciating and long-lasting neurologic pain.

“This trial is important because it demonstrates that the vaccine works in severely immuno suppressed patients,” said oncologist Keith Sullivan, M.D., the James B. Wyngaarden Professor of Medicine at Duke. “That suggests it could also work with others whose immune systems are not normal — including patients with HIV, breast cancer and auto-immune conditions.”

Sullivan and colleagues at 167 centers in 28 countries enrolled more than 1,800 transplant recipients. Half were randomly assigned to received two vaccine doses shortly after transplant and half received placebo. 

At a median follow-up of 21 months, the vaccine group had 30 cases of shingles per 1,000 person-years compared to 94 cases per 1,000 person-years among patients receiving placebo injections.

The vaccine also apparently reduced the incidence of painful post-therapeutic neuralgia, shingles-related hospitalizations and complications and duration of pain. 

“Among HSCT patients, a shingles outbreak is often more feared than the transplant itself, and I’ve had patients tell me they’d undergo two transplants before facing another episode of shingles,” Sullivan said. “It’s hugely gratifying, and a welcome surprise, to see such a strong immune response among this study population.”

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In addition to Sullivan, study authors include Adriana Bastidas, Javier de la Serna, Mohamed El Idrissi, Lidia Oostvogels, Philippe Quittet, Javier López-Jiménez, Filiz Vural, David Pohlreich, Tsila Zuckerman, Nicolas C. Issa, Gianluca Gaidano, Je-Jung Lee, Sunil Abhyankar, Carlos Solano, Jaime Perez de Oteyza, Michael J. Satlin, Stefan Schwartz, Magda Campins, Alberto Rocci, Carlos Vallejo Llamas, Dong-Gun Lee, Sen Mui Tan, Anna M. Johnston, Andrew Grigg, Michael J. Boeckh, Laura Campora, Marta Lopez-Fauqued, Thomas C. Heineman and Edward A. Stadtmauer for the ZOE-HSCT Study Group Collaborators.

Sullivan has received grants and personal fee from GSK, which markets the vaccine and sponsored the study.