Endogenous cytokine production protects T cells from spontaneous apoptosis during highly active antiretroviral therapy

F. Ensoli, V. Fiorelli, M. De Cristofaro, B. Collacchi, D. Santini Muratori, C. Alario, G. Sacco, F. Iebba, F. Aiuti

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Background. The availability of therapeutic regimens that effectively interfere with HIV-1 replication provides novel opportunities to investigate mechanisms of T-cell depletion as well as repopulation in infected individuals. Methods. Nineteen HIV-1-infected individuals were investigated during one-year follow-up of highly active retroviral therapy (HAART). The frequencies of apoptotic T cells, as determined by propidium iodide, staining, TUNEL assay and analysis of annexin V, were assessed either in the absence or in the presence of anti-interleukin (IL)2 and anti-IL-4 neutralizing Ab. Spontaneous and lectin-induced cytokine production were assessed by ELISA. Results. Increments of both naive and memory CD4 and CD8 T cells during HAART are accompanied by a decrease of T-cell apoptosis that, after 12 months of HAART, reaches normal levels. This is associated with increments of both spontaneous and activation-induced production of IL-2 and IL-4 by peripheral blood mononuclear cells (PBMCs), though only the latter was found defective at enrolment. During HAART, blocking of either IL-2 or IL-4 production by PBMCs using neutralizing Ab restores levels of T-cell apoptosis consistent with those determined at enrolment. These data suggest that both IL-2 and IL-4 produced by PBMCs during HAART provide anti-apoptotic signals that can contribute to an increased survival of T cells and may thus play a part in long-term immune reconstitution. Conclusions. An effective viral suppression and, possibly, effects of PI on molecular targets other than viral components, can support a progressive normalization of T-cell survival that, at least in part, depends upon the restoration of proper soluble signals. These results provide evidence of a supporting role of endogenous cytokine production in peripheral T-cell repopulation during an effective and prolonged viral suppression. This may be relevant for the definition of immune-intervention targets aimed at immune reconstitution in HIV-1-infected patients.

Original languageEnglish
Pages (from-to)105-117
Number of pages13
JournalHIV Medicine
Volume3
Issue number2
DOIs
Publication statusPublished - 2002

Fingerprint

Highly Active Antiretroviral Therapy
Apoptosis
Cytokines
T-Lymphocytes
Interleukin-4
Interleukin-2
HIV-1
Blood Cells
Viral Structures
Propidium
Annexin A5
In Situ Nick-End Labeling
Lectins
Cell Survival
Enzyme-Linked Immunosorbent Assay
Staining and Labeling
Therapeutics

Keywords

  • AIDS/HIV
  • Apoptosis
  • Cytokines
  • Th1/Th2

ASJC Scopus subject areas

  • Immunology
  • Virology
  • Medicine(all)

Cite this

Endogenous cytokine production protects T cells from spontaneous apoptosis during highly active antiretroviral therapy. / Ensoli, F.; Fiorelli, V.; De Cristofaro, M.; Collacchi, B.; Santini Muratori, D.; Alario, C.; Sacco, G.; Iebba, F.; Aiuti, F.

In: HIV Medicine, Vol. 3, No. 2, 2002, p. 105-117.

Research output: Contribution to journalArticle

Ensoli, F, Fiorelli, V, De Cristofaro, M, Collacchi, B, Santini Muratori, D, Alario, C, Sacco, G, Iebba, F & Aiuti, F 2002, 'Endogenous cytokine production protects T cells from spontaneous apoptosis during highly active antiretroviral therapy', HIV Medicine, vol. 3, no. 2, pp. 105-117. https://doi.org/10.1046/j.1468-1293.2002.00107.x
Ensoli, F. ; Fiorelli, V. ; De Cristofaro, M. ; Collacchi, B. ; Santini Muratori, D. ; Alario, C. ; Sacco, G. ; Iebba, F. ; Aiuti, F. / Endogenous cytokine production protects T cells from spontaneous apoptosis during highly active antiretroviral therapy. In: HIV Medicine. 2002 ; Vol. 3, No. 2. pp. 105-117.
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AU - Fiorelli, V.

AU - De Cristofaro, M.

AU - Collacchi, B.

AU - Santini Muratori, D.

AU - Alario, C.

AU - Sacco, G.

AU - Iebba, F.

AU - Aiuti, F.

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