Stanford study finds potential shingles prevention in a childhood vaccine

July 03, 2002

STANFORD, Calif., July 1, 2002 - Stanford researchers have found that a childhood vaccine given in adulthood can reduce the risk of shingles, an excruciatingly painful disease that strikes the elderly and people with weakened immune systems.

Researchers studied the effects of an inactivated form of the chicken pox vaccine in cancer patients who were especially likely to develop shingles (also called zoster). It appears possible that the vaccination can prevent healthy elderly people from developing the disease and that other vaccines might be a good way to protect transplant recipients against viruses and bacteria.

"We knew that these patients were at very high risk for zoster," said Ann Arvin, chief of pediatric infectious disease at Lucile Packard Children's Hospital. "We thought we could try to benefit those with impaired immune systems, and also demonstrate that vaccination could help protect others who are at risk for shingles."

Arvin, a professor of microbiology and immunology, is the senior author of the study, which will be published in the New England Journal of Medicine Thursday. Karl Blume, MD, professor of medicine and chief of the division of bone marrow transplantation at Stanford University Medical Center is a co-investigator.

Shingles is triggered by the same virus that causes chicken pox. While most people recover from chicken pox without incident, the virus then bides its time in nerve cells - a nefarious stowaway, waiting decades for a chance to strike again. When the immune system is weakened by age or disease, the virus springs to life, spurring an itchy, burning rash and a legacy of shooting pain that can last for years.

"It's a very disruptive kind of pain," said Arvin, "The skin becomes so sensitive that it can be difficult to sleep and even the lightest clothing or faint breeze becomes painful." Arvin estimates that even for healthy adults the risk of shingles rises each decade after age 60, increasing to one in five for people in their 80s.

Researchers tested the effect of an inactivated version of the chicken pox vaccine on lymphoma patients about to undergo a hematopoietic cell transplant to combat cancer. Because these patient's immune systems are weakened by the disease and its treatment, up to one third of them develop shingles within 12 months of their transplant. Using an inactivated vaccine reduced the chance of adverse side effects in the study subjects.

Arvin and her colleagues found that only 13 percent of the 53 patients who received one dose of the inactivated vaccine within 30 days prior to the transplant, followed by three additional doses after transplant, developed shingles. On the other hand, 30 percent of the 56 participants in the unvaccinated control group got the disease.

The key appears to be the pre-transplant treatment; a previous study by Arvin that tested only post-transplant vaccination showed no protection. This indicates that some immunity must remain even after the patient's immune system is wiped out during the transplant procedure.

"We would suggest from our data that the same pre-transplant vaccination strategy would work to protect these patients against other viruses and bacteria," said Arvin. "The idea that they are so immunocompromised that you can't benefit these patients by vaccination during the early stage of the transplant is incorrect."

Researchers suspect that the protection against shingles is conferred by memory T cells - virus-specific immune cells jump-started by the vaccine to mount an attack during the transplant and subsequent recovery. When they rated the strength of the T cell immune response to the virus at various times during the transplant, they found that patients in both the vaccinated and unvaccinated groups who went on to develop shingles shared especially low levels of immunity. Those whose T cells responded more strongly to the virus were less likely to develop shingles. Vaccination increased the T cell response to the virus and protected against shingles.
Lucile Salter Packard Children's Hospital at Stanford is a 240-bed hospital devoted entirely to the care of children and expectant mothers that is celebrating its tenth anniversary in 2001. Providing pediatric medical and surgical services associated with Stanford University Medical Center, Packard offers patients locally, regionally and nationally with the full range of health care programs and services - from preventive and routine care to the diagnosis and treatment of serious illness and injury. To learn more about Lucile Packard Children's Hospital, please visit our Web site at

Stanford University Medical Center

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