Tuberculous Effusion: ADA Activity Correlates with CD4+ Cell Numbers in the Fluid and the Pleura

Respiration ◽  
2005 ◽  
Vol 72 (2) ◽  
pp. 160-165 ◽  
Author(s):  
M. Gaga ◽  
G. Papamichalis ◽  
P. Bakakos ◽  
P. Latsi ◽  
I. Samara ◽  
...  
Keyword(s):  
1992 ◽  
Vol 66 (3) ◽  
pp. 1484-1488 ◽  
Author(s):  
G Hoffmann-Fezer ◽  
J Thum ◽  
C Ackley ◽  
M Herbold ◽  
J Mysliwietz ◽  
...  

2003 ◽  
Vol 71 (2) ◽  
pp. 956-963 ◽  
Author(s):  
Tammy A. Myers ◽  
Janet E. Leigh ◽  
Alfredo R. Arribas ◽  
Shannon Hager ◽  
Rebecca Clark ◽  
...  

ABSTRACT Oropharyngeal candidiasis (OPC), caused by Candida albicans, is the most frequent opportunistic fungal infection in human immunodeficiency virus (HIV)-positive persons. Although Th1-type CD4+ T cells are considered important for host defense against mucosal C. albicans infections, there is a paucity of information regarding the presence and/or role of T cells in OPC lesions. In pursuit of this, initial chromophore immunohistochemical studies showed a majority of CD8+ rather than CD4+ cells equally distributed throughout the buccal mucosa of OPC− persons (HIV− or HIV+), irrespective of blood CD4+ cell numbers. In contrast, CD8+ cells in lesions from HIV+ OPC+ persons were in significantly higher numbers and concentrated at the lamina propria-epithelium interface, a considerable distance from the Candida at the outer epithelium. Dual fluorescence and confocal microscopy confirmed that the majority of CD8+, but not CD4+, cells were T cells by the presence or absence, respectively, of CD3 on each cell type. These results suggest that CD8+ T cells may be important for oral host defense against OPC, especially when CD4 cell numbers are reduced, with a potential CD8 cell-specific dysfunction associated with susceptibility to OPC.


2009 ◽  
Vol 409 (1-2) ◽  
pp. 4-10 ◽  
Author(s):  
Seetharamaiah Chittiprol ◽  
Adarsh M. Kumar ◽  
K. Taranath Shetty ◽  
H. Ravi Kumar ◽  
P. Satishchandra ◽  
...  

2007 ◽  
Vol 120 (4) ◽  
pp. 960-962 ◽  
Author(s):  
Kanami Orihara ◽  
Masami Narita ◽  
Takashi Tobe ◽  
Akira Akasawa ◽  
Yukihiro Ohya ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Ruth Pia Duecker ◽  
Lucia Gronau ◽  
Patrick C. Baer ◽  
Stefan Zielen ◽  
Ralf Schubert

Hematopoietic stem cell transplantation (HSCT) has been proposed as a promising therapeutic opportunity to improve immunity and prevent hematologic malignancies in Ataxia-telangiectasia (A-T). However, experience in the transplantation strategy for A-T patients is still scarce. The aim of this study was to investigate whether different approaches of HSCT are feasible in regard to graft versus host response and sufficient concerning functional immune reconstitution. Atm-deficient mice were treated with a clinically relevant non-myeloablative host-conditioning regimen and transplanted with CD90.2-depleted, green fluorescent protein (GFP)-expressing, and ataxia telangiectasia mutated (ATM)-competent bone marrow donor cells in a syngeneic, haploidentical or allogeneic setting. Like syngeneic HSCT, haploidentical HSCT, but not allogeneic HSCT extended the lifespan of Atm-deficient mice through the reduction of thymic tumors and normalized T-cell numbers. Donor-derived splenocytes isolated from transplanted Atm-deficient mice filled the gap of cell loss in the naïve T-cell population and raised CD4 cell functionality up to wild-type level. Interestingly, HSCT using heterozygous donor cells let to a significantly improved survival of Atm-deficient mice and increased CD4 cell numbers as well as CD4 cell functionality equivalent to HSCT using with wild-type donor cells. Our data provided evidence that haploidentical HSCT could be a feasible strategy for A-T, possibly even if the donor is heterozygous for ATM. However, this basic research cannot substitute any research in humans.


1988 ◽  
Vol 4 (6) ◽  
pp. 433-440 ◽  
Author(s):  
FRANK DE WOLF ◽  
MARIJKE ROOS ◽  
JOEP M.A. LANGE ◽  
JOSÉ T.M. HOUWELING ◽  
ROEL A. COUTINHO ◽  
...  
Keyword(s):  
Cd4 Cell ◽  

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