1985
DOI: 10.1016/s0166-3542(85)80037-1
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Booster vaccination of healthy adults with VZV antibody but without a VZV-specific cell-mediated immune response

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Cited by 12 publications
(3 citation statements)
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“…The first trial of Berger et al in 33 subjects showed that 17 vaccinees developed a strong VZV-specific LPA response, and 11 developed a weak response [5]. The second Berger trial chose subjects on the basis of a negative VZV skin test, a procedure that is probably immunizing in its own right and would complicate evaluation of the vaccine [3].…”
Section: Clinical Trials With Candidate Hz Vaccinesmentioning
confidence: 99%
“…The first trial of Berger et al in 33 subjects showed that 17 vaccinees developed a strong VZV-specific LPA response, and 11 developed a weak response [5]. The second Berger trial chose subjects on the basis of a negative VZV skin test, a procedure that is probably immunizing in its own right and would complicate evaluation of the vaccine [3].…”
Section: Clinical Trials With Candidate Hz Vaccinesmentioning
confidence: 99%
“…11 Varicella-zoster virus-specific, cell-mediated immunity is enhanced by vaccination with live, attenuated VZV vaccination. 12 In addition, researchers have demonstrated that VZV vaccination enhances both humoral and cellular VZV-specific immune responses. 13 Following vaccination with zoster vaccine live, VZV antibody levels are increased.…”
Section: Pharmacologymentioning
confidence: 99%
“…21 Pilot studies indicated that VZV CMI could be boosted in subjects 60 to >90 years of age by administration of investigational live attenuated Oka/Merck VZV vaccines. 15,21,22,[27][28][29][30][31] Following preliminary trials to assess the safety and immunogenicity of an investigational high potency live attenuated Oka/Merck VZV vaccine ("zoster vaccine") in elderly subjects, including persons with diabetes or chronic obstructive lung disease, and to establish optimal vaccine formulation and potency (Levin, Oxman et al, unpublished), a large double blind, placebo controlled clinical trial ("The Shingles Prevention Study") was carried out in older adults to test the ability of zoster vaccine to decrease the Burden of Illness due to HZ and reduce the Incidence of PHN. 16 The Shingles Prevention Study (SPS) was a VA Cooperative Study carried out in collaboration with the National Institute of Allergy and Infectious Diseases and Merck & Co., Inc., with the approval of a Human Rights Committee of the VA Cooperative Studies Program and Institutional Review Boards at each of 22 study sites across the United States; each subject provided written Vaccination to Prevent Herpes Zoster and Postherpetic Neuralgia informed consent.…”
mentioning
confidence: 99%