Article Text


Impairment of β chemokine and cytokine production in patients with HIV related Pneumocystis jerovici pneumonia
  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;


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

Statistics from

HIV related mortality and morbidity have fallen dramatically since the introduction of highly active antiretroviral therapy (HAART), but the incidence of Pneumocystis jerovici pneumonia (PJP) remains relatively stable. PJP is still the most common AIDS revealing opportunistic infection in patients unaware of their HIV seropositivity. PJP is an independent risk factor for HIV disease progression, partly because it triggers intense viral replication1–7 through unknown mechanisms.8–10 Some inflammatory mediators known to upregulate HIV replication are produced during PJP and tuberculosis.11,12 However, anti-inflammatory mediators that potently inhibit HIV replication are normally produced both in vitro and in animal models.13–15 In vivo, HIV replication is tightly controlled by a balance between pro- and anti-inflammatory cytokines.16,17 An imbalance between these mediators during the course of PJP would lead to a failure to control HIV replication in the lung and to a net increase in viral load. This issue has never, to our knowledge, been investigated. However, clues to the mechanisms by which PJP upregulates viral replication could have important therapeutic implications, such as the use of specific biological response modifiers. We have therefore examined the HIV load and pro- and anti-inflammatory cytokine and chemokine production in patients with active PJP.


Study population

Bronchoalveolar lavage (BAL) was performed as part as the routine work up of HIV seropositive patients with unexplained fever, whether or not they had pulmonary symptoms or infiltrative lung disease. Patients were informed that a part of the pathological specimens could be used for molecular analysis provided that a definitive pathological diagnosis was obtained on their BAL fluid samples. BAL was performed in the most affected lung segment identified by CT scanning. Specimens were examined microscopically for cytological abnormalities, fungi and parasites, and were cultured for bacteria (including mycobacteria), fungi, parasites and viruses. Protected brush specimens were also obtained from patients with purulent secretions or focal abnormalities. When standard staining revealed no pathogens, BAL fluid specimens were tested for P jerovici and Toxoplasma gondii by immunofluorescence.

Forty patients were enrolled in this retrospective study between February 1995 and February 1997. The above procedures revealed isolated PJP in 23 patients and ruled out opportunistic lung infection in 17 patients with isolated fever. At the time of BAL, 15 patients were receiving one or two antiretroviral drugs and 25 patients were receiving no antiretroviral treatment. When possible, aliquots of cell free BAL supernatants were stored at −80°C for HIV load assay.

Table 1 shows the age, sex, HIV transmission group, CD4 cell count, and antiretroviral treatment of the study patients and table 2 shows the BAL findings.

Table 1

Characteristics of study patients

Table 2

Mean (SE) bronchoalveolar lavage cell composition (%)

Bronchoalveolar cell culture

BAL fluid remaining after the diagnostic tests was centrifuged (200 g, 4°C, 10 min) and the cell pellet was resuspended in RPMI 1640 culture medium (ATGC, Noisy le Grand, France). Cell were >95% viable in the Trypan blue exclusion test. Cell density was adjusted to 1×106/ml in RPMI medium supplemented with 1% FCS (Flow, Les Ulis, France), 1% glutamine, and 1% penicillin-streptomycin (GIBCO, BRL, Eragny, France), and 106 cells were cultured overnight in polypropylene tubes at 37°C with 5% CO2. After 18–20 hours, cell free culture supernatants were recovered and stored at −80°C until analysis (within 18 months).

Viral load assay

The HIV-1 RNA level in cell free BAL fluid and in concomitant serum samples was measured with a commercial reverse transcription polymerase chain reaction (RT-PCR) kit (HIV Monitor, Roche Molecular Diagnostic Systems, Meylan, France; detection limit: 50 HIV-1 RNA copies/ml). To compensate for the dilution of epithelial lining fluid during the BAL procedure, alveolar viral load was corrected for the BAL fluid albumin concentration.

Cytokine and chemokine assays

Concentrations of cytokines and chemokines known to upregulate (TNFα, IL-6) or downregulate (IL-10, RANTES, MIP-1α, MIP-1β) HIV replication in vitro were measured in plasma and in BAL cell culture supernatants. Commercially available ELISA kits were used from R&D Systems (Abingdon, UK) for RANTES, MIP-1α and MIP-1β and from Biosource Europe (Nivelle, Belgium) for IL-6, IL-10 and TNFα. Results are expressed in pg/ml plasma or culture supernatant. The detection limits of the kits are 10, 4, and 4 pg/ml, respectively, for RANTES, MIP-1α and MIP-1β; and 2, 1, and 3 pg/ml, respectively, for IL-6, IL-10 and TNFα.

Statistical analysis

Results are expressed as median (range). Comparisons were made using the non-parametric Mann-Whitney U test. Distributions of values were compared between groups using the χ2 test. Correlations were identified using the Spearman rank test. p values of <0.05 were considered significant.


Viral load in BAL fluid and plasma

Plasma viral load did not differ significantly between the patients with or without PJP: 63 735 (5262–380 882) v 6534 (199–300 311) copies/ml, respectively. In contrast, the viral load in BAL fluid was markedly higher in patients with PJP than in those without, whether expressed per ml or per mg albumin: 2003 (366–19 013) v 277 (200–479) copies/ml, respectively (p<0.05); 47 250 (4690–322 256) v 3519 (1150–6746) copies/mg albumin, respectively (p<0.01). In the patients with PJP the viral load was, on average, 17 times higher in BAL fluid than in plasma: 47 250 (4690–322 256) v 2826 (195–15 870) copies/mg albumin, respectively (p<0.001; fig 1A) with a strong positive correlation between the two (r = 0.832, p<0.001). In addition, the viral load was higher in BAL fluid than in plasma in all patients with PJP (fig 1B). Taken together, these data suggest local viral production, with alveolar lymphocytes possibly being the main source. Indeed, the viral load in the BAL fluid was positively correlated with the percentage of lymphocytes present in BAL fluid (r = 0.322, p<0.05) and with no other cell type. In contrast, in subjects not infected with PJP the viral load did not differ significantly between BAL fluid and plasma: 3519 (1150–6746) v 272 (5–8385) copies/mg albumin, respectively. In the BAL fluid the viral load was not correlated with the amount of any cell type present.

Figure 1

(A) HIV viral load in bronchoalveolar lavage (BAL) fluid (solid bars) and plasma (shaded bars) of the patient group with PJP and those free of PJP (controls). (B) Individual values of viral load of patients in the two groups (open circles, plasma levels; closed circles, BAL fluid); *p<0.001.

Proinflammatory cytokine and chemokine production by cultured alveolar cells

Spontaneous release of the proinflammatory cytokines TNFα and IL-6 by cultured BAL cells was similar in patients without or with PJP: 1880 (1000–2150) v 1840 (1077–2385) pg TNFα/ml, respectively (NS); 2295 (1492–3461) v 2280 (1729–3521) pg IL-6/ml, respectively (NS; fig 2). By contrast, BAL cells from patients with PJP spontaneously produced far less IL-10 and β-chemokines than BAL cells from patients without PJP. On average, BAL cells from patients with PJP produced three times less IL-10 than cells from patients without PJP: 24 (5–85) v 75 (40–170) pg/ml (p<0.01; fig 3A); in addition, IL-10 production by BAL cells was undetectable in 11 (58%) of the 19 tested subjects with PJP but was detected in all nine subjects tested who were free of PJP (p<0.01, χ2 test). The viral load in the BAL fluid correlated positively with IL-6 release from BAL fluid cells (r = 0.220, p<0.05) and negatively with IL-10 release from BAL fluid cells (r = 0.380, p<0.01).

Figure 2

Production of IL-6 and TNFα by alveolar cells in patients without PJP (shaded bars) and those with PJP (solid bars).

Figure 3

Production by alveolar cells of (A) IL-10, (B) RANTES, (C) MIP-1α, and (D) MIP-1β in patients with PJP (solid bars) and those without PJP (shaded bars); *p<0.001.

Beta-chemokine production by alveolar cells also appeared to be markedly defective in the PJP group. RANTES production was six times lower in patients with PJP than in those without PJP: 58 (20–120) v 357 (105–720) pg/ml, respectively (p<0.001; fig 3B) and was undetectable in five (26%) of 19 subjects tested with PJP but was detectable in all nine patients tested without PJP. Likewise, MIP-1α production was six times lower in subjects with PJP: 202 (90–355) v 1117 (680–1725) pg/ml, respectively (p<0.001; fig 3C) and was below the detection limit in four of the 14 (29%) tested subjects with PJP and in none of the nine PJP free subjects tested. Although MIP-1β was produced by BAL cells from all the subjects in both groups the levels were 10 times lower in the PJP group: 87 (19–370) v 900 (90–1220) pg/ml, respectively (p<0.001; fig 3D). Beta-chemokine production by BAL cells correlated negatively with the BAL fluid viral load in the overall population (r = 0.215, p<0.05 for both MIP-1α and RANTES).

Proinflammatory cytokine and chemokine plasma levels

Plasma concentrations of TNFα and IL-6 did not differ significantly between patients with or without PJP: 24 (3–139) v 23 (3–119) pg TNFα/ml and 13 (2–201) v 3(2–56) pg IL-6/ml, respectively (NS; fig 4A and B). Plasma IL-10 concentrations were also similar in the two groups: 195 (45–485) v 205 (25–500) pg/ml (NS; fig 4C). In contrast, plasma β-chemokine levels were far lower in the PJP group than in the PJP free group, in keeping with the situation observed in the lung. The difference was highly significant for RANTES (27 494 (19 114–38 763) v 47 830 (9881–209 930) pg/ml in patients with and without PJP, respectively; p<0.001) and for MIP-1β (51 (21–75) v 78 (26–153) pg/ml in patients with and without PJP, respectively; p<0.002). MIP-1α plasma levels tended to be lower in the PJP group (14 (6–40) v 20 (4–61) pg/ml; NS).

Figure 4

Plasma levels of (A) TNFα, (Β) IL-6 and (C) IL-10 were comparable whereas those of (D) RANTES and (F) MIP-1β were significantly decreased (*p<0.002) in patients with PJP (solid bars) compared with those free of PJP (shaded bars). Plasma levels of MIP-1α (E) were lower in patients with PJP, although not significantly.


To our knowledge, this is the first study to show that increased HIV replication in the lungs of subjects with active PJP is linked to both strongly defective local β-chemokine release and an imbalance between proinflammatory and anti-inflammatory cytokine production. Opportunistic infections known to promote HIV replication1–3 include both active tuberculosis4,9 and PJP.5–7,10 In our study PJP was associated with a markedly higher viral load in BAL fluid but not in plasma, suggesting active pulmonary viral replication. In addition, the viral load in the BAL fluid and plasma were correlated strongly with each other in the PJP group (p<0.001) but not in the PJP free control group, suggesting that viral production triggered in the lung by P jerovici infection may make a strong contribution to the circulating viral load. The difference in pulmonary viral load between the two groups cannot be explained by different treatment strategies as similar proportions of patients were untreated at the time of the study (78% and 72% of subjects with and without PJP, respectively), while the remainder were on single or dual agent antiretroviral regimens.

Several factors might be involved in the increased local virus production triggered by opportunistic pulmonary pathogens. Firstly, pathogen constituents could have a direct impact on HIV gene transcription. For example, Mycobacterium tuberculosis upregulates HIV replication both in vitro and in vivo,4,8,18 while Mycobacterium avium facilitates HIV infection of monocyte derived macrophages in vitro and is associated with pronounced viral replication in lymph nodes of HIV co-infected patients.19 To our knowledge, no direct effect of P jerovici on HIV transcriptional mechanisms has been reported.

Opportunistic pathogens are also known to facilitate HIV replication indirectly by upregulating inflammatory mediators9–11 such as TNFα and IL-6.20–23 Several in vitro studies have shown a direct effect of some P jerovici constituents on TNFα release.24,25 We and others have shown that PJP is associated with marked production of proinflammatory cytokines, particularly TNFα, in the human lung.12,26 A direct effect of proinflammatory cytokines on HIV production has been clearly established in vitro but not in vivo.26,27 In this study we found that spontaneous TNFα and IL-6 release by alveolar cells in vitro was similar in subjects with and without PJP. Thus, the markedly higher pulmonary viral load associated with PJP is probably due to other mechanisms, potentially including deficient IL-10 and β-chemokine production. Indeed, the balance between proinflammatory and anti-inflammatory cytokines is known to influence the replication of HIV critically.16,17

IL-10 has complex effects on HIV infection. In vivo, high plasma levels of IL-10 have been linked to more rapid HIV disease progression.28,29 In vitro, IL-10 inhibits HIV replication in macrophages30 but also cooperates with TNFα to activate HIV replication.31 The latter effect was also recently observed with latently infected T cells.32 IL-10 has complex regulatory effects on HIV expression which depend on its own concentration and on the presence of other HIV regulatory cytokines (particularly TNFα and IL-6).33 We found a negative correlation between IL-10 release by BAL cells and pulmonary viral load. IL-10 is a potent Th2 (anti-inflammatory) cytokine which exerts negative regulatory effects on Th1 (proinflammatory) cytokines by downregulating their synthesis,34 at least partly through specific mRNA destabilisation.35 IL-10 is strongly released in the lungs of experimental animals with PJP36 and also in humans.37 In our study, IL-10 levels were similar in the plasma of subjects with and without PJP, but were far lower in BAL fluid of subjects with PJP than in PJP free controls. We have no clear explanation for these findings. The strong influence of IL-10 gene promoter polymorphisms on the pattern of IL-10 production38 cannot explain the compartmentalisation of this defective production. Whatever the mechanism, the reduced capacity of alveolar cells to produce IL-10 during PJP would lead to a relative excess of Th1 cytokines, which are produced during the acute phase of pneumonia and markedly upregulate virus replication.

The rate of HIV replication is also influenced by the balance between the inductive effects of some endogenous cytokines (TNFα and IL-1) and the suppressive effects of others;13,17,39,40 RANTES is the most potent chemokine in this respect.41 In vivo, high circulating levels of MIP-1β have been linked to a lesser risk of HIV disease progression.42 It is therefore noteworthy that alveolar cells isolated from our patients with PJP displayed a markedly decreased capacity to release β-chemokines in culture, and that this release correlated negatively with the viral load in the BAL fluid. To our knowledge, this is the first report of such a defect in the context of PJP. Alveolar cells from HIV infected patients may exhibit impaired chemokine release on stimulation with lipopolysaccharide, a defect that correlates with the number of circulating CD4 cells.43 Intracellular MIP-1β accumulates in HIV infected subjects, with a negative relationship between the intracellular and secreted forms which is strongly linked to the degree of immunodeficiency.44 SCID mice challenged with P jerovici show no pulmonary inflammatory response (partly owing to their inability to produce chemokines), while immune reconstitution leads to an intense response at the site of pulmonary infection together with strong local production of chemokines, particularly RANTES.14 The reduced capacity of our patients to generate an efficient chemokine response might therefore be due partly to their severe immunodeficiency. Alternatively, the defective chemokine production could be due to a direct effect of P jerovici, in the same way as previously suggested in HIV infected patients with pleural tuberculosis.9 Beta-chemokines suppress HIV replication through competitive binding to their cell surface receptor (CCR5) which is also a key HIV co-receptor for macrophage-tropic virus entry, particularly in the lungs.45 Interestingly, HIV and some opportunistic pathogens upregulate the expression of chemokine receptors on infected alveolar macrophages.45 CCR5, for instance, is strongly upregulated during the course of M tuberculosis infection, both in vivo and in vitro.9,15,46,47 These effects are thought to be involved in the impact of tuberculosis on HIV infection.48 It would be interesting to examine CCR5 expression by BAL fluid cells from patients with PJP. Together with deficient chemokine production, CCR5 enhancement might leave a large number of HIV co-receptors unoccupied on lung cells. A concomitant imbalance in proinflammatory/anti-inflammatory cytokine production could result in transcriptional activation of HIV in latently infected cells and facilitate HIV infection of newly recruited cells. Moreover, activated macrophages are highly susceptible to classically T-tropic strains of HIV49,50 owing to their strong expression of CCR3 and CXCR4.45 By a combination of these mechanisms, PJP might create one of the most propitious situations for HIV replication and dissemination.


View Abstract

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.