Abstract |
Multicentric Castleman disease (MCD) is a rare human herpes virus type 8 (HHV8)-associated lymphoproliferative disorder that occurs more frequently in patients infected with human immunodeficiency virus (HIV). In tissue samples, HHV8-infected plasmablasts localise to the mantle zones of the lymphoid follicles. We revisited the immunohistological features in 25 lymph node (LN) and three spleen samples of MCD. In five (20%) LN and one (33%) spleen sample, HHV8 latent nuclear antigen 1 (LANA1) staining was also noted on the follicular dendritic cells (FDC). The HHV8-positive FDC subgroup of patients had significantly higher numbers of CD3-positive T cells infiltrating the follicles when compared to the HHV8-negative FDC subgroup (P = 0.047). Furthermore, the numbers of HHV8-positive plasmablasts and serum HHV8 viral copy numbers were lower among the HHV8-positive FDC subgroup when compared to the HHV8-negative FDC subgroup (not statistically significant). Our findings show, for the first time, possible 'presentation' of an HHV8 antigen by FDCs in MCD.
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Authors | Hesham El-Daly, Mark Bower, Kikkeri N Naresh |
Journal | European journal of haematology
(Eur J Haematol)
Vol. 84
Issue 2
Pg. 133-6
(Feb 01 2010)
ISSN: 1600-0609 [Electronic] England |
PMID | 19799625
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Antigens, Viral
- CD3 Complex
- Nuclear Proteins
- latency-associated nuclear antigen
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Topics |
- Adult
- Aged
- Antigens, Viral
(immunology, metabolism)
- CD3 Complex
(immunology, metabolism)
- Castleman Disease
(complications, immunology, metabolism, pathology, virology)
- Dendritic Cells
(immunology, metabolism, pathology, virology)
- Female
- HIV
(immunology, metabolism)
- HIV Infections
(complications, immunology, metabolism, pathology, virology)
- Herpesviridae Infections
(complications, immunology, metabolism, pathology, virology)
- Herpesvirus 8, Human
(immunology, metabolism)
- Humans
- Lymph Nodes
(immunology, metabolism, pathology, virology)
- Male
- Middle Aged
- Nuclear Proteins
(immunology, metabolism)
- Spleen
(immunology, metabolism, pathology, virology)
- T-Lymphocytes
(immunology, metabolism, pathology, virology)
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