| Literature DB >> 23074274 |
Susan Moir1, Suk See De Ravin, Brian H Santich, Jin Young Kim, Jacqueline G Posada, Jason Ho, Clarisa M Buckner, Wei Wang, Lela Kardava, Mary Garofalo, Beatriz E Marciano, Jody Manischewitz, Lisa R King, Surender Khurana, Tae-Wook Chun, Hana Golding, Anthony S Fauci, Harry L Malech.
Abstract
CD27(+) memory B cells are reduced in the blood of patients with chronic granulomatous disease (CGD) for reasons and consequences that remain unclear. Here we confirm not only decreased CD27(+) but also IgG(+) B cells in the blood of CGD patients compared with healthy donors (HDs). However, among IgG(+) B cells, the ratio of CD27(-) to CD27(+) was significantly higher in CGD patients compared with HDs. Similar to conventional memory B cells, CD27(-)IgG(+) B cells of CGD patients expressed activation markers and had undergone somatic hypermutation, albeit at levels lower than their CD27(+) counterparts. Functional analyses revealed slight reductions in frequencies of total IgG but not influenza-specific memory B-cell responses, as measured by Elispot in CGD patients compared with HDs. Serum IgG levels and influenza-specific antibodies were also normal in these CGD patients. Finally, we provide evidence that influenza-specific memory B cells can be present within the CD27(-)IgG(+) B-cell compartment. Together, these findings show that, despite reduced circulating CD27(+) memory B cells, CGD patients maintain an intact humoral immunologic memory, with potential contribution from CD27(-) B cells.Entities:
Mesh:
Substances:
Year: 2012 PMID: 23074274 PMCID: PMC3520621 DOI: 10.1182/blood-2012-05-430959
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113