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Impairment of β chemokine and cytokine production in patients with HIV related Pneumocystis jerovici pneumonia
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  1. D Israël-Biet1,2,
  2. H Esvant1,
  3. A M Laval1,
  4. J Cadranel3
  1. 1Laboratoire d’Immunopathologie Pulmonaire, UPRES EA220, Université Paris V, Paris, France
  2. 2Service de Pneumologie, Hôpital Européen Georges Pompidou, Paris, France
  3. 3Service de Pneumologie et de Réanimation respiratoire, Hôpital Tenon, Paris, France
  1. Correspondence to:
    Professor D Israël-Biet
    Service de Pneumologie, Hôpital Européen Georges Pompidou, 20 rue Leblanc, 75015 Paris, France; dib.laennecinvivo.edu

Abstract

Background:Pneumocystis jerovici pneumonia (PJP) remains a frequent opportunistic infection in HIV infected patients which markedly upregulates HIV replication by mechanisms so far poorly elucidated. PJP triggers the production of proinflammatory mediators with activating effects on HIV. However, anti-inflammatory factors with inhibiting effects on HIV are normally produced in parallel. We postulated that an imbalance of mediators normally controlling HIV replication could underlie its marked increase during PJP.

Methods: The production of tumour necrosis factor α (TNFα), interleukins IL-6 and IL-10, and β-chemokine by bronchoalveolar lavage (BAL) cells recovered from HIV infected patients with and without PJP was compared. The pulmonary viral load was determined and correlations with cytokine and chemokine production were examined.

Results: TNFα and IL-6 release was similar in patients with and without PJP but IL-10 and β-chemokine release was markedly lower in the PJP group (IL-10: p<10−2, RANTES, MIP-1α and MIP-1β: p<0.001). The pulmonary viral load was markedly higher in patients with PJP (p<0.001) and correlated negatively with levels of MIP-1α, RANTES and IL-10 in BAL fluid cells (p<0.05).

Conclusion: Pulmonary IL-10 and β-chemokine production is markedly defective in HIV infected patients with PJP, while pulmonary TNFα and IL-6 levels are normal. The resulting excess of these latter factors, which are known to upregulate HIV replication, might contribute to the increase in pulmonary viral load and to the more rapid HIV disease progression observed in patients with PJP.

  • Pneumocystis jerovici pneumonia
  • HIV infection
  • cytokines
  • chemokines
  • IL, interleukin
  • MIP, macrophage inflammatory protein
  • PJP, Pneumocystis jerovici pneumonia
  • RANTES, regulated on activation normal T cell expressed and secreted
  • TNF, tumour necrosis factor

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