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Blood, 15 November 2001, Vol. 98, No. 10, pp. 3016-3021
IMMUNOBIOLOGY
Reduced blood CD123+ (lymphoid) and
CD11c+ (myeloid) dendritic cell numbers in
primary HIV-1 infection
Jérôme Pacanowski,
Sandrine Kahi,
Marjorie Baillet,
Pierre Lebon,
Christiane Deveau,
Cécile Goujard,
Laurence Meyer,
Eric Oksenhendler,
Martine Sinet, and
Anne Hosmalin
From Unité INSERM 445, Immunologie des
pathologies infectieuses et tumorales, Département
d'Immunologie, Institut Cochin de Génétique
Moléculaire and Laboratoire de Virologie, Hôpital
St-Vincent de Paul, Paris, France; Unité INSERM 292, PRIMO Cohort
Study Group, Equipe INSERM E0109, Immunité antivirale
systémique et cérébrale, and Service de
Médecine Interne, Hôpital de Bicêtre, Le
Kremlin-Bicêtre, France; and Service d'Immuno-Hématologie,
Hôpital St Louis, Paris; France.
Successful immunologic control of HIV infection is achieved only in
rare individuals. Dendritic cells (DCs) are required for specific antigen presentation to naive T lymphocytes and for antiviral, type I interferon secretion. Two major blood DC populations are found:
CD11c+ (myeloid) DCs, which secrete IL-12, and
CD123+ (IL-3-receptor+) DCs (lymphoid), which
secrete type I interferons in response to viral stimuli. The authors
have previously found a decreased proportion of blood
CD11c+ DCs in chronic HIV+ patients. In this
study, 26 to 57 days after infection and before treatment,
CD123+ and CD11c+ DC numbers were dramatically
reduced in 13 HIV+ patients compared with 13 controls
(P = .0002 and P = .001,
respectively). After 6 to 12 months of highly active
antiretroviral therapy, DC subpopulation average numbers remained low,
but CD123+ DC numbers increased again in 5 of 13 patients.
A strong correlation was found between this increase and CD4 T-cell
count increase (P = .0009) and plasma viral load decrease
(P = .009). Reduced DC numbers may participate in the
functional impairment of HIV-specific CD4+ T cells
and be responsible for the low type I interferon responsiveness already
known in HIV infection. The restoration of DC numbers may be
predictive of immune restoration and may be a goal for immunotherapy to
enhance viral control in a larger proportion of patients.

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