TY - JOUR
T1 - Prevalence and distribution of VZV in temporal arteries of patients with giant cell arteritis
AU - Gilden, Don
AU - White, Teresa
AU - Khmeleva, Nelly
AU - Heintzman, Anna
AU - Choe, Alexander
AU - Boyer, Philip J.
AU - Grose, Charles
AU - Carpenter, John E.
AU - Rempel, April
AU - Bos, Nathan
AU - Kandasamy, Balasubramaniyam
AU - Lear-Kaul, Kelly
AU - Holmes, Dawn B.
AU - Bennett, Jeffrey L.
AU - Cohrs, Randall J.
AU - Mahalingam, Ravi
AU - Mandava, Naresh
AU - Eberhart, Charles G.
AU - Bockelman, Brian
AU - Poppiti, Robert J.
AU - Tamhankar, Madhura A.
AU - Fogt, Franz
AU - Amato, Malena
AU - Wood, Edward
AU - Durairaj, Vikram
AU - Rasmussen, Steve
AU - Petursdottir, Vigdis
AU - Pollak, Lea
AU - Mendlovic, Sonia
AU - Chatelain, Denis
AU - Keyvani, Kathy
AU - Brueck, Wolfgang
AU - Nagel, Maria A.
N1 - Publisher Copyright:
© 2015 American Academy of Neurology.
PY - 2015/5/12
Y1 - 2015/5/12
N2 - Objective: Varicella-zoster virus (VZV) infection may trigger the inflammatory cascade that characterizes giant cell arteritis (GCA). Methods: Formalin-fixed, paraffin-embedded GCA-positive temporal artery (TA) biopsies (50 sections/TA) including adjacent skeletal muscle and normal TAs obtained postmortem from subjects >50 years of age were examined by immunohistochemistry for presence and distribution of VZV antigen and by ultrastructural examination for virions. Adjacent regions were examined by hematoxylin & eosin staining. VZV antigen-positive slides were analyzed by PCR for VZV DNA. Results: VZV antigen was found in 61/82 (74%) GCA-positive TAs compared with 1/13 (8%) normal TAs (p < 0.0001, relative risk 9.67, 95% confidence interval 1.46, 63.69). Most GCA-positive TAs contained viral antigen in skip areas. VZV antigen was present mostly in adventitia, followed by media and intima. VZV antigen was found in 12/32 (38%) skeletal muscles adjacent to VZV antigen-positive TAs. Despite formalin fixation, VZV DNA was detected in 18/45 (40%) GCA-positive VZV antigen-positive TAs, in 6/10 (60%) VZV antigen-positive skeletal muscles, and in one VZV antigen-positive normal TA. Varicella-zoster virions were found in a GCA-positive TA. In sections adjacent to those containing VZV, GCA pathology was seen in 89% of GCA-positive TAs but in none of 18 adjacent sections from normal TAs. Conclusions: Most GCA-positive TAs contained VZV in skip areas that correlated with adjacent GCA pathology, supporting the hypothesis that VZV triggers GCA immunopathology. Antiviral treatment may confer additional benefit to patients with GCA treated with corticosteroids, although the optimal antiviral regimen remains to be determined.
AB - Objective: Varicella-zoster virus (VZV) infection may trigger the inflammatory cascade that characterizes giant cell arteritis (GCA). Methods: Formalin-fixed, paraffin-embedded GCA-positive temporal artery (TA) biopsies (50 sections/TA) including adjacent skeletal muscle and normal TAs obtained postmortem from subjects >50 years of age were examined by immunohistochemistry for presence and distribution of VZV antigen and by ultrastructural examination for virions. Adjacent regions were examined by hematoxylin & eosin staining. VZV antigen-positive slides were analyzed by PCR for VZV DNA. Results: VZV antigen was found in 61/82 (74%) GCA-positive TAs compared with 1/13 (8%) normal TAs (p < 0.0001, relative risk 9.67, 95% confidence interval 1.46, 63.69). Most GCA-positive TAs contained viral antigen in skip areas. VZV antigen was present mostly in adventitia, followed by media and intima. VZV antigen was found in 12/32 (38%) skeletal muscles adjacent to VZV antigen-positive TAs. Despite formalin fixation, VZV DNA was detected in 18/45 (40%) GCA-positive VZV antigen-positive TAs, in 6/10 (60%) VZV antigen-positive skeletal muscles, and in one VZV antigen-positive normal TA. Varicella-zoster virions were found in a GCA-positive TA. In sections adjacent to those containing VZV, GCA pathology was seen in 89% of GCA-positive TAs but in none of 18 adjacent sections from normal TAs. Conclusions: Most GCA-positive TAs contained VZV in skip areas that correlated with adjacent GCA pathology, supporting the hypothesis that VZV triggers GCA immunopathology. Antiviral treatment may confer additional benefit to patients with GCA treated with corticosteroids, although the optimal antiviral regimen remains to be determined.
UR - http://www.scopus.com/inward/record.url?scp=84929207753&partnerID=8YFLogxK
U2 - 10.1212/WNL.0000000000001409
DO - 10.1212/WNL.0000000000001409
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C2 - 25695965
AN - SCOPUS:84929207753
SN - 0028-3878
VL - 84
SP - 1948
EP - 1955
JO - Neurology
JF - Neurology
IS - 19
ER -