4.7 Article

Altered expression of the receptor-ligand pair CXCR5/CXCL13 in B cells during chronic HIV-1 infection

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BLOOD
卷 112, 期 12, 页码 4401-4410

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AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2008-02-140426

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资金

  1. Swedish Research Council (MRC)
  2. Swedish International Development Agency
  3. Regione Autonoma della Sardegna, Cagliari, Italy
  4. Istituto Italiano di Cultura C. M. Lerici Foundation, Stockholm, Sweden
  5. German Ministry of Education and Research
  6. Compentence Network for HIV/AIDS [FKZ 01KI0501]
  7. Stockholm County Council
  8. Karolinska Institutet
  9. EU

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HIV-1 infection is associated with B-cell abnormalities, such as hypergamma-globulinemia, poor immunization responses, and loss of serologic memory. To determine whether altered expression of chemokine receptors and their ligands may play a role in B-cell dysfunctions during HIV-1 infection, the expression of CXC chemokine receptor 4 (CXCR4), CXCR5, and CC chemokine receptor 7 (CCR7) and their respective ligands on CD19(+) B cells were examined in HIV-1-infected patients and controls. We report a decreased CXCR5 expression on B cells from patients (P < .05), a phenomenon associated with a low CD4 T-cell count (< 350 cells/mu L). Interestingly, an increased expression of CXC chemokine ligand 13 (CXCL13), the ligand for CXCR5, was found in peripheral B cells from HIV-1-infected patients. Moreover, on B-cell activation in vitro, CXCL13 was secreted in culture. CXCL13(+) B cells were also found in the lymph nodes of HIV-1-infected patients, but not in control tissue. B-cell migration toward CXCL13, CXCL12, and CC chemokine ligand 21 (CCL21), ligands for CXCR5, CXCR4, and CCR7 was also evaluated. In patients with a low CD4 T-cell count, migration toward all ligands was increased. Our findings indicate that altered expression of the chemokine receptor-ligand pair, CXCR5/ CXCL13, may participate in the establishment of B-cell dysfunctions during HIV-1 infection. (Blood. 2008;112:4401-4410)

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