Persistently High Antibody Titers and Deficient Specific Cellular Immunity to Varicella-Zoster Virus in a Retarded Patient after Varicella Infection

1992 ◽  
Vol 34 (4) ◽  
pp. 459-465
Author(s):  
Kihei Terada ◽  
Shoji Kawano ◽  
Kiyomi Yoshihiro ◽  
Tetsuro Morita
Blood ◽  
1990 ◽  
Vol 75 (3) ◽  
pp. 806-809 ◽  
Author(s):  
S Kato ◽  
H Yabe ◽  
M Yabe ◽  
M Kimura ◽  
M Ito ◽  
...  

Abstract The transfer of antigen-specific cellular immunity in human bone marrow transplantation (BMT) was studied in 49 donor-recipient pairs, using a varicella-zoster-virus (VZV) specific lymphoproliferative response (LPR) assay. Posttransplant VZV-LPR could be serially measured in 31 long-term surviving recipients. VZV-specific T-cell immunity was detected in the early posttransplant period in 4 of 16 recipients who were, and whose donors were, immune to VZV before BMT, but two of those positive responses diminished in the first 100 days posttransplant. No positive response was detected in the immediate posttransplant period when either only the recipient or the donor was immune to VZV pretransplant. Herpes zoster or chickenpox developed in the recipients depending on a history of pretransplant VZV infection when the VZV-LPR became negative, and recovery from VZV infection was always followed by quick conversion of VZV-LPR. Long-lasting positive VZV-LPR was observed in the two recipients who experienced VZV infection in the immediate pretransplant period and received marrow graft from an immune donor. Our results indicate that a simple or direct transfer of VZV-specific cellular immunity from a marrow donor to a recipient cannot be expected in usual clinical bone marrow transplantation and that there might be a collaboration or recruitment of immune responses involving both donor and recipient that permits the VZV-LPR to remain positive posttransplant.


2005 ◽  
Vol 94 (6) ◽  
pp. 790-793 ◽  
Author(s):  
Teresa Murguía-de-Sierra ◽  
Mónica Villa-Guillén ◽  
Dina Villanueva-García ◽  
Antide Molina ◽  
Alejandra Juárez-Chávez ◽  
...  

2014 ◽  
Vol 211 (4) ◽  
pp. 600-612 ◽  
Author(s):  
David Schub ◽  
Eva Janssen ◽  
Sarah Leyking ◽  
Urban Sester ◽  
Gunter Assmann ◽  
...  

1999 ◽  
Vol 180 (3) ◽  
pp. 834-837 ◽  
Author(s):  
Takuji Kumagai ◽  
Makoto Kamada ◽  
Chiharu Igarashi ◽  
Kenji Yuri ◽  
Hidetsugu Furukawa ◽  
...  

1978 ◽  
Vol 8 (6) ◽  
pp. 733-735
Author(s):  
A A Gershon ◽  
S Piomelli ◽  
M Karpatkin ◽  
E Smithwick ◽  
S Steinberg

Antibody titers to varicella-zoster virus were measured in varicella-susceptible immunocompromised children 48 h after they received either one of two lots of zoster immune globulin (ZIG) or a selected lot of immune serum globulin (ISG). Globulin was given to modify varicella in these children after exposure to varicella or zoster. Indirect immunofluorescence antibody titers (FAMA) of children after receipt of globulin ranged from less than 1:2 to 1:32. Geometric mean FAMA titers were highest after 1.2 ml of ISG per kg (FAMA titer 1:128) and 0.16 ml of ZIG lot A per kg (FAMA titer 1:1,024). Selected batches of ISG titering 1:128 or greater by FAMA, at a dose of 1.2 ml/kg, may be used to attempt to modify varicella in susceptible high-risk individuals when ZIG is not available.


1998 ◽  
Vol 178 (s1) ◽  
pp. S104-S108 ◽  
Author(s):  
Michael Irwin ◽  
Carolyn Costlow ◽  
Heather Williams ◽  
Kamal Haydari Artin ◽  
Christina Y. Chan ◽  
...  

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