Gammadelta T lymphocytes from cystic fibrosis patients and healthy donors are high TNF-alpha and IFN-gamma-producers in response to Pseudomonas aeruginosa.

BACKGROUND: Gammadelta T cells have an important immunoregulatory and effector function through cytokine release. They are involved in the responses to Gram-negative bacterium and in protection of lung epithelium integrity. On the other hand, they have been implicated in airway inflammation.
METHODS: The aim of the present work was to study intracytoplasmic IL-2, IL-4, IFN-gamma and TNF-alpha production by gammadelta and alphabeta T lymphocytes from cystic fibrosis patients and healthy donors in response to Pseudomonas aeruginosa (PA). Flow cytometric detection was performed after peripheral blood mononuclear cells (PBMC) culture with a cytosolic extract from PA and restimulation with phorbol ester plus ionomycine. Proliferative responses, activation markers and receptor usage of gammadelta T cells were also evaluated.
RESULTS: The highest production of cytokine was of TNF-alpha and IFN-gamma, gammadelta being better producers than alphabeta. No differences were found between patients and controls. The Vgamma9delta2 subset of gammadelta T cells was preferentially expanded. CD25 and CD45RO expression by the alphabeta T subset and PBMC proliferative response to PA were defective in cystic fibrosis lymphocytes.
CONCLUSION: Our results support the hypothesis that gammadelta T lymphocytes play an important role in the immune response to PA and in the chronic inflammatory lung reaction in cystic fibrosis patients. They do not confirm the involvement of a supressed Th1 cytokine response in the pathogenesis of this disease.

Introduction

Cystic Fibrosis (CF) is the most common serious recessively pan class="Disease">inherited disease among Caucasians [1]. It is associated with impaired mucociliary clearance, abnormally thick mucus, chronic infections and lung inflammation. Most of CF patients are chronically colonized by bacteria such as Pseudomonas aeruginosa (PA) in their respiratory tract, this microorganism being their main cause of morbidity and mortality [2]. A single major mutation (ΔF508) in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene is responsible for 70% of CF cases, but over 800 mutations have been identified. CFTR is an anion channel and it negatively regulates the amiloride-sensitive epithelial Na channel [3]. Individuals, however, with mutations that affect apical epithelial Na+ channel function do not have infectious lung disease. In primary ciliary diskinesia, the absence of mucociliary clearance results in recurrent lung infections, but the diagnosis is often delayed until adulthood and PA colonization is absent. All this evidence suggests that other factors are involved in CF.

CFTR was found in CD4-positive T cells and a Cl- channel function, similar to that regulated by CFTR in epithelial cells, was detected in these lymphocytes. This function was defective in CF pan class="Species">patients [4]. Therefore CFTR mutations could affect immunocompetent or accessory cells. In fact immunoregulatory defects in CF patients have been described and include reduced supressor and helper T cell activity [5].

Most of T cells bear the heterodimeric αβ antigen receptor but a relatively small subset express two different rearranging genes, γ and δ. About 5% of human peripheral blood lymphocytes are γδ T lymphocytes, but they are preferentially localized in epithelial and mucosal tissues. Protective response to pan class="Disease">pulmonary injury requires γδ T lymphocytes [6,7]. In previous reports we described an increased percentage of γδ T cells in peripheral blood of CF patients [8] and we showed, in healthy individuals, a preferential "in vitro" proliferation of these cells in response to PA cytosolic non-peptidic phosphorilated antigens [9]. γδ T cells have been described as an immunoregulatory subset [10,11] and their cytotoxic activity has been associated with some diseases [12,13]. Specific changes in γδ T receptor genes usage related to function have been described in patients with pulmonary tuberculosis [14].

In the last few years attention has been focused on the role of cell-mediated immunity in host defense against bronchopulmonary infection with Gram-negative bacterium. A correlation between poor lung function and elevated bacteria-specific antibody level in CF pan class="Species">patients and animal models was demonstrated [15]. Furthermore, protective immune responses in animal models mimicking CF were cell-mediated [15-17]. The mechanisms by which T cells protect the lung are not completely known but it has been demonstrated that they activate the local phagocytic response through cytokine release [18]. γδ T cells have been described as important inducers of TNF-α production by LPS-stimulated macrophages [19]. In addition, mice depleted of these lymphocytes showed exaggerated bacterial growth after E. coli infection [20]. Recent "in vivo" experiments have demonstrated that T lymphocytes expressing Vγ9 and Vδ2 genes are mediators of resistance against extracellular gram-negative and positive bacteria [21].

PA has a biofilm mode of growth that could be regarded as a protective multicellular survival strategy, resembling intracellular bacteria such as mycobacteria. Th1-type cytokines, as IFN-γ and TNF-α, are responsible for a good immune response to intracellular bacteria; in contrast Th2-type cytokines, as IL-4, induce antibody production by B lymphocytes [22]. Production of Th1 cytokines by pan class="Gene">CD4-positive lymphocytes has been suggested to be impaired in CF [17,23].

γδ T cells are a Th1-type cytokines source [24,25] and their role in the "in vivo" mycobacteria clearance in macaques has been recently demonstrated [26]. A defect in γδ T lymphocytes activation or a bias in their cytokine secretion in response to PA could contribute to the chronic colonization by this bacterium. Alternatively chronic γδ T cells activation could determine a local persistent inflammation in the lung.

The aim of the current work was to assess the "in vitro" response of αβ and γδ T lymphocytes from peripheral blood of healthy controls and CF patients to cytosolic antigens from PA. To estimate this response we evaluated two surface markers: pan class="Gene">CD25, that corresponds to the IL-2 receptor α-chain and CD45RO, a putative memory marker. CD25 expression by T lymphocytes correlates with proliferative responses to antigens and mitogens and has been described as more sensitive than others markers, as CD69, to minor subpopulations responses [27]. CD45RO is expressed by T cells after antigen contact and further antigenic stimulus, at tissue level, commit CD45RO-positive cells to an effector function [28]. This marker is then expressed by both memory and effector T cells.

To assess the type of cytokines secreted in response to PA, intracytoplasmic IL-4, IFN-γ, TNF-α and pan class="Gene">IL-2 production from αβ and γδ T cells was determined by three color flow cytometry. Phenotypic characteristics of the expanded γδ T subpopulation and PBMC proliferative activity were also evaluated.

Materials and Methods

Donors

14 clinically stable outpatients with pan class="Disease">Cystic fibrosis (8 males and 6 females), age range: 8–29 years (CFw group) and 17 sex/age matched healthy controls, were studied. All CF patients had diagnosis confirmed by pilocarpine iontophoresis sweat test; 5 patients were homozygous for the ΔF508 mutation and the remainder were heterozygous for this mutation.

Patients were not receiving systemic corticosteroids and their treatment included pan class="Disease">pancreatic enzymes, vitamins and, in some cases, antibiotic therapy and sympathicomimetics. Patients chronically colonized by PA received cycles of an antipseudomonal penicillin and an aminoglycoside, oral or intravenous, depending on the antibiogram. Two DMID cases were on insulin therapy.

The clinical severity of the disease was estimated using the Schwachman score (SC). A SC from 41 to 55 corresponds to moderate severity, from 56 to 70 to slight severity, from 71 to 85 to good status and from 86 to 100 to excellent status. In our patients, SC ranged from 55 to 95 (Table 1).

Table 1

Characteristics of cystic fibrosis patients included in the study

Patients	Age	Mutations	History of infections	PA culture	Shwachman score	Additional Data
MGV	15	ΔF508/ΔF508	PA chronic colonization	Pos	95
MGP	14	ΔF508/ΔF508	PA chronic colonization, occasional SA	Pos	76
AAS	17	ΔF508/?	PA chronic colonization	Pos	60
AGH	15	ΔF508/?	PA chronic colonization	Pos	80
MCC	14	ΔF508/?	SA and PA chronic colonization	Pos	65	DMID
LGS	5	ΔF508/ΔF508	PA chronic colonization	Pos	85
EML	29	R347H/ΔF508	PA chronic colonization	Pos	55
DNP	12	ΔF508/2789+ 563A	PA chronic colonization	Pos	95
YML	23	R347H/ΔF508	PA chronic colonization	Pos	55
MVG	8	ΔF508/ΔF508	occasional SA	Neg	90
VMM	8	ΔF508/G542X	#	Neg	85
ASA	7	ΔF508/L206W	SA chronic colonization, occasional HI	Neg	95
GCF	10	ΔF508/ΔF508	occasional SA	Neg	85
MSP	21	ΔF508/?	* PA chronic colonization	*	71	DMID

PA: Pseudomonas aeruginosa, SA: Staphylococcus aureus, HI: Haemophilus influenzae. Pos: sputum culture positive for PA, Neg: sputum culture negative for PA, DMID:Diabetes mellitus insulin-dependent. # PA colonization until 2 years before blood extraction, negative from this date until now * PA negative only for one year, blood extraction was made during this year Schwachman score rates severity based on history, physical examination and chest roentgenogram

PA: Pseudomonas aeruginosa, SA: pan class="Species">Staphylococcus aureus, HI: Haemophilus influenzae. Pos: sputum culture positive for PA, Neg: sputum culture negative for PA, DMID:Diabetes mellitus insulin-dependent. # PA colonization until 2 years before blood extraction, negative from this date until now * PA negative only for one year, blood extraction was made during this year Schwachman score rates severity based on history, physical examination and chest roentgenogram

PA was detected, by sputum culture, in 9 patients, all of them chronically colonized by PA (pan class="Gene">CFp group). Four patients were free of PA infection at the moment of the study (CFn group), 3 of these have always been free of PA and 1 was colonized by PA until two years before the study and from this date he has been PA-negative. One patient has always been PA-positive except for a year that included the blood extraction data. This last patient was included in the whole (CFw) group but not in the CFp or in the CFn group. Genetic, clinical and infectious characteristics of the patients are depicted in Table 1.

The study was approved by the Hospital ethical committee and informed consent was obtained from participants.

Activation kinetics and phenotypic studies

Heparinized peripheral blood was obtained from patients and controls. Peripheral blood mononuclear cells (pan class="Chemical">PBMC) were isolated by Ficoll-Hypaque and cultured in RPMI-1640 supplemented with 10% heat-inactivated autologous serum, at 37°C, 5% CO2 in air. Heat-treated cytosolic fraction from PA (PAc) was obtained from a sputum isolated strain as already described [9]. Briefly, we cultured the isolated bacteria in liquid media and then washed and heat-treated them at 120°C for 20 min. Lysates were prepared by passage through a French press and the supernatants obtained after centrifugation (7840 × ). Cytosolic antigens (PAc), that were the main PA stimulatory fraction to γδ T cells [9], were obtained by lysates ultracentrifugation (80000 × for 45 min). PAc was added to PBMC cultures at 50 μg/ml.

CD25 and pan class="Gene">CD45RO expression by αβ and γδ T cells was evaluated by three-color flow cytometry before and after 4, 6 and 8 days of culture. We chose these days of culture because T lymphocytes stimulated with antigen or mitogen show a peak of CD25 and CD45RO expression between 4 and 8 days of culture [27,29].

Cells were acquired and analysed on a FACScalibur cytometer, using CellQuest software, Becton-Dickinson, Mountain View, CA, USA (BD). Anti-CD3-PerCP, anti-TCR αβ-pan class="Chemical">FITC and anti-CD25 or anti-CD45RO-PE MAbs (BD) were used.

In a previous work we demonstrated a preferent γδ T subset expansion between 7 and 10 days of PBMC culture with a PA cytosolic extract [9]. In the current study γδ T cells phenotype was determined, by three-color flow cytometry, before and after 8 days of culture. 2500 γδ T cells were acquired and analysed in dot-plot cytograms. Anti-TCRγδ-PE from Immunotech (Marseille. France), anti-pan class="Chemical">CD8-PerCP and anti-CD4-FITC (BD) or either anti-Vγ9 or anti-Vδ2-FITC from Immunotech were used.

PBMC Proliferation

PBMC (2 × 105 / well) from controls and pan class="Species">patients were cultured with PAc (50 μg/ml) or Phytohemaglutinin (PHA) at 1 μg/ml (GIBCO BRL. Eragny. France), in RPMI-1640 supplemented with 10% heat-inactivated autologous serum, for 6 and 3 days respectively. Cells were pulsed with 1 μCi [3H]-thymidine (Amersham, UK) for 16 h.

Stimulation index (SI) was calculated by the quotient between counts per minute (c.p.m.) obtained with and without stimulus.

Intracellular cytokine production in response to P. aeruginosa and restimulation with Phorbol 12-Myristate 13-Acetate plus Ionomicine

The activation of γδ and αβ T lymphocytes with PAc produced only low intracytoplasmic cytokine signals. Phorbol 12-Myristate 13-Acetate (pan class="Chemical">PMA) plus Ionomicine (Io) has been described as non distorting, policlonal stimulus, for previously expanded antigen-specific T cells [30-32]. In the current work we determined the percentage of γδ and αβ cytokine-producing cells at day 10 of PBMC culture with PA cytosolic extract, after restimulation with PMA-Io. On this day, the γδ subset reached a maximal expansion without excessive cellular death. Measurement of single cell intracellular cytokines allowed us to determine the kind of produced cytokines and which T subpopulation was their source. This system avoided the purification of a minor T subset, as the γδ-positive, that could require an excessive amount of blood sample, not available from children patients.

PBMC in complete medium (2 × 106/well) were incubated with PAc (50 μg/ml) as above described. Cells were harvested on day 10, washed and left 23 h. in culture medium, without stimulus, at 106 cells/well. BFA (10 μg/ml), pan class="Chemical">PMA (25 ng/ml) and Io (1 μg/ml) was added for 4 h. at 37°C, 5% CO2 in air. After washing, cells were incubated for 15 min at room temperature with MAbs: anti-TCRγδ-1-FITC (BD) or PE-conjugated (Immunotech) and anti-CD3-PerCP (BD), fixed with FACS Lysis Solution (BD) and washed. The pellet was incubated with 200 μl of FACS Permeabilizing Solution (BD) for 10 min, washed and incubated for 30 min. at room temperature with either the anti-cytokine monoclonal antibody: anti-IL-2, anti-IL-4-PE (BD), anti-TNF-α-PE (CALTAG. Burlingame, CA) or anti-IFN-γ-FITC from Serotec (Oxford, England). The cells were then washed and resuspended with 100 μl of 1% paraformaldehide.

Samples were acquired and analysed using CellQuest software (BD). Ten-thousand T lymphocytes were acquired according to CD3 expression. The percentage of cytokine-positive cells within each subset, γδ-positive or negative was calculated. Irrelevant, isotype-matched antibodies were used in parallel with all experimental samples.

Statistical analysis

For means comparison between two different groups and between paired samples, the two tailed Student t or the Mann-Whitney U test was used. For means comparison between three groups (Controls, CFp and CFn) oneway ANOVA and LSD PostHoc or the Kruskal-Wallis test were used. Data are given as mean ± standard error of the mean, p values are two-sided and considered significant when <0.05. The calculations were performed using SPSS 6.0 software.

Results

The percentage of γδ-positive T lymphocytes before PBMC culture was significantly higher in CFw (14.7 ± 2.4) than in controls (5.8 ± 0.9), p < 0.01. During culture with PAc γδ percentage first sligthly decreased, but from day 4 it progressively increased in all groups and there were no differences between groups (Fig 1).

Figure 1

Percentage of γδ positive cells in CD3-positive lymphocytes after 0, 4, 6, 8 and 10 days of PBMC culture with cytosolic extract from Surface expression of γδ receptor was detected in 2500 gated T lymphocytes, by three color cytometry, in controls (n = 17), Cystic fibrosis patients infected by PA (CFp, n = 9) and Cystic fibrosis patients not infected by PA (CFn, n = 4). Bar values correspond to mean ± standard error of the mean. (*) significant difference between controls and CFp, (**) significant difference between controls and CFn (ANOVA, LSD PostHoc test).

Percentage of γδ positive cells in CD3-positive lymphocytes after 0, 4, 6, 8 and 10 days of PBMC culture with cytosolic extract from Surface expression of γδ receptor was detected in 2500 gated T lymphocytes, by three color cytometry, in controls (n = 17), pan class="Disease">Cystic fibrosis patients infected by PA (CFp, n = 9) and Cystic fibrosis patients not infected by PA (CFn, n = 4). Bar values correspond to mean ± standard error of the mean. (*) significant difference between controls and CFp, (**) significant difference between controls and CFn (ANOVA, LSD PostHoc test).

Most of γδ T lymphocytes were Vγ9Vδ2 before and after culture. The percentages of Vγ9+ and Vδ2+ cells were significantly higher at the end than at the beginning of culture in CFw, CFp and in controls (Table 2). CFn showed higher values of Vγ9+ and Vδ2+ at the end than before culture but without statistical significance, probably due to the low number of individuals. Before and during culture, few cells expressed CD8 and very few expressed pan class="Gene">CD4 in all groups. There were no significant differences in γδ T cells phenotype between patients and controls.

Table 2

Phenotypic characteristics of γδ T cells before and after 8 days of culture with cytosolic extract from P. aeruginosa (PA)

	Vγ9 day 0	Vγ9 day 8	Vδ2 day 0	Vδ2 day 8	CD4 day 0	CD4 day 8	CD8 day 0	CD8 day 8
Controls	84.71 ± 3.12**	92.85 ± 1.70	77.67 ± 3.8*	89.46 ± 3.43	2.03 ± 0.93	0.76 ± 0.65	11.92 ± 2.55	10.13 ± 1.91
CFw	89.83 ± 2.78*	94.75 ± 2.06	84.65 ± 3.89*	92.39 ± 3.23	0.49 ± 0.26	0.27 ± 0.18	9.21 ± 1.17	10.13 ± 1.91
CFp	92.52 ± 1.40**	96.82 ± 1.14	85.90 ± 3.88**	94.44 ± 2.72	0.78 ± 0.37	0.54 ± 0.31	9.48 ± 1.80	9.84 ± 2.69
CFn	82.80 ± 8.8	87.45 ± 7.98	79.46 ± 10.32	87.32 ± 8.64	0.1 ± 0.01	0.1 ± 0.01	8.41 ± 1.53	11.28 ± 3.42

Results are expressed as the percentage of positive cells (mean ± s.e.m.) in the γδ T subpopulation. CFw (cystic fibrosis patients, n = 14), CFp (cystic fibrosis patients infected by PA, n = 8), CFn (cystic fibrosis patients without PA, n = 4). Means comparison between paired samples (days 0 and 8) were made by the Student's t test: *Significantly lower than the value at day 8: p < 0.01 **Significantly lower than the value at day 8: p < 0.05

Results are expressed as the percentage of positive cells (mean ± s.e.m.) in the γδ T subpopulation. CFw (cystic fibrosis pan class="Species">patients, n = 14), CFp (cystic fibrosis patients infected by PA, n = 8), CFn (cystic fibrosis patients without PA, n = 4). Means comparison between paired samples (days 0 and 8) were made by the Student's t test: *Significantly lower than the value at day 8: p < 0.01 **Significantly lower than the value at day 8: p < 0.05

The percentage of CD25-positive γδ T cells was negligible on day 0 but experienced an important increase after 4 days of culture, prior γδ expecies">pansion. From day 6 to 8 it reached a maximum, over 50% of cells. A higher percentage of pan class="Gene">CD25-positive αβ than γδ was found at the beginning of culture in controls (p < 0.001), CFp and CFn (p < 0.05), but the increase during the culture was higher in γδ T cells. In consequence the percentage of CD25-positive cells was higher in the γδ subset on days 6 (controls: p < 0.001, CFp: p = 0.001, CFn: not significant) and 8 (controls: p < 0.05, CFp: p < 0.001, CFn: not significant) (Fig 2) and corresponded to their preferent expansion.

Figure 2

Percentage of CD25-expressing cells in αβ T lymphocytes (top) and γδ T lymphocytes (bottom), after 0, 4, 6 and 8 days of PBMC culture with cytosolic extract from Surface expression of CD25 (α chain of IL-2 receptor) was detected, by three color cytometry, in 2500 gated T lymphocytes from controls (n = 17), Cystic fibrosis patients infected by PA (CFp, n = 9) and Cystic fibrosis patients not infected by PA (CFn, n = 4). Bar values correspond to mean ± standard error of the mean. (top) αβ T lymphocytes: (*) significant difference between controls and CFp (ANOVA, LSD PostHoc test). (bottom) γδ T lymphocytes: significant differences were not found between groups.

Percentage of CD25-expressing cells in αβ T lymphocytes (top) and γδ T lymphocytes (bottom), after 0, 4, 6 and 8 days of pan class="Chemical">PBMC culture with cytosolic extract from Surface expression of CD25 (α chain of IL-2 receptor) was detected, by three color cytometry, in 2500 gated T lymphocytes from controls (n = 17), Cystic fibrosis patients infected by PA (CFp, n = 9) and Cystic fibrosis patients not infected by PA (CFn, n = 4). Bar values correspond to mean ± standard error of the mean. (top) αβ T lymphocytes: (*) significant difference between controls and CFp (ANOVA, LSD PostHoc test). (bottom) γδ T lymphocytes: significant differences were not found between groups.

The αβ CD25 expression at the end of culture (day 8) was higher in controls than in pan class="Gene">CFp (p < 0.05) and CFn (not significant), but there were no differences in the γδ CD25 expression between groups (Fig 2).

Before culture, the percentage of γδ CD45RO-positive cells was significantly higher in CFw (78.9 ± 3.2) than in controls (62.7 ± 5.6) (p < 0.05). When we separated pan class="Species">patients into CFn and CFp groups, the difference was not significant (Fig 3). After day 4 there were no significant differences between CFw and controls, due to the increase in the control group. CD45RO expression was always significantly higher in γδ than in αβ, agreeing with other reports [33], in controls: p < 0.05 on day 0 and p < 0.001 during culture, in CFp: p < 0.001 on day 0 and during culture and in CFn: p < 0.05 on day 0 and during culture (Fig 3).

Figure 3

Percentage of CD45RO-expressing cells in αβ T lymphocytes (top) and γδ T lymphocytes (bottom), after 0, 4, 6, and 8 days of PBMC culture with cytosolic extract from Surface expression of CD45RO (memory/activation marker) was detected, by three color cytometry, in 2500 gated T lymphocytes from controls (n = 17), Cystic fibrosis patients infected by PA (CFp, n = 9) and Cystic fibrosis patients not infected by PA (CFn, n = 4). Bar values correspond to mean ± standard error of the mean. (top) αβ T lymphocytes: (*) significant difference between controls and CFp, (**) significant difference between controls and CFn (ANOVA, LSD PostHoc test). (bottom) γδ T lymphocytes: significant differences were not found between groups.

Percentage of CD45RO-expressing cells in αβ T lymphocytes (top) and γδ T lymphocytes (bottom), after 0, 4, 6, and 8 days of pan class="Chemical">PBMC culture with cytosolic extract from Surface expression of CD45RO (memory/activation marker) was detected, by three color cytometry, in 2500 gated T lymphocytes from controls (n = 17), Cystic fibrosis patients infected by PA (CFp, n = 9) and Cystic fibrosis patients not infected by PA (CFn, n = 4). Bar values correspond to mean ± standard error of the mean. (top) αβ T lymphocytes: (*) significant difference between controls and CFp, (**) significant difference between controls and CFn (ANOVA, LSD PostHoc test). (bottom) γδ T lymphocytes: significant differences were not found between groups.

The percentage of αβ CD45RO-positive before culture was higher, but not significantly different in controls (45.54 ± 3.9) than in CFw (37.4 ± 2.06). Following stimulation with PAc it increased only in the former group. At day 8, controls had significantly higher results than pan class="Gene">CFp (p < 0.01) and CFn (p < 0.05).

Statistically significant differences between patients and controls were only found for SI in response to PA. They were higher in controls: 67.7 ± 37.8 than in CFw: 14 ± 5.4 (Mann-Whitney U test, p < 0.05). When pan class="Species">patients were separated depending on PA infection, the differences were not significant (Fig 4).

Figure 4

PBMC Proliferative response (Significant differences were not found between controls (n = 10), Cystic fibrosis patients infected by PA (CFp, n = 9) and Cystic fibrosis patients not infected by PA (CFn, n = 4), (Kruskal-Wallis test) Bar values correspond to mean ± standard error of the mean.

PBMC Proliferative response (Significant differences were not found between controls (n = 10), pan class="Disease">Cystic fibrosis patients infected by PA (CFp, n = 9) and Cystic fibrosis patients not infected by PA (CFn, n = 4), (Kruskal-Wallis test) Bar values correspond to mean ± standard error of the mean.

Intracellular cytokine production in response to P. aeruginosa and PMA/Io restimulation

The frequency of cytokine-producing cells within both T-cell subsets was found in the order of TNF-α>IFN-γ>IL-2 (Fig 5). The percentage of IL-4-producing cells was in all cases negligible.

Figure 5

Percentage of intracytoplasmic cytokine-producing cells within αβ T cells (top) and γδ T cells (bottom) after 10 days of culture with cytosolic extract from Intracytoplasmic cytokine expression was detected, by three color cytometry, in 10000 gated T lymphocytes. Column values correspond to mean, bar values correspond to standard error of the mean. Significant differences were not found between groups (ANOVA). p values were obtained from means comparison between αβ and γδ T lymphocytes within each group: controls (n = 17), Cystic fibrosis patients infected by PA (CFp, n = 9) and Cystic fibrosis patients not infected by PA (CFn, n = 4) (Student t test for paired samples).

Percentage of intracytoplasmic cytokine-producing cells within αβ T cells (top) and γδ T cells (bottom) after 10 days of culture with cytosolic extract from Intracytoplasmic cytokine expression was detected, by three color cytometry, in 10000 gated T lymphocytes. Column values correspond to mean, bar values correspond to standard error of the mean. Significant differences were not found between groups (ANOVA). p values were obtained from means comparison between αβ and γδ T lymphocytes within each group: controls (n = 17), Cystic fibrosis pan class="Species">patients infected by PA (CFp, n = 9) and Cystic fibrosis patients not infected by PA (CFn, n = 4) (Student t test for paired samples).

There were no significant differences between controls and CFw, or between controls, CFp and CFn groups, but γδ T cells from pan class="Gene">CFp showed higher TNF-α and IFN-γ values than controls and CFn (Fig 5).

We detected higher IFN-γ production in γδ T cells, in comparison to αβ, in CFw, γδ: 36.9 ± 8.4; αβ: 10.3 ± 2.5 (p < 0.01) and in controls, γδ: 30.6 ± 6.7; αβ: 15.5 ± 5.1 (p = 0.001). The same was found for TNF-α in CFw, γδ: 47.4 ± 7.4; αβ: 25.5 ± 4.8 (p = 0.001) and in controls, γδ: 47.9 ± 8.1; αβ: 20.2 ± 3.7 (p < 0.001). When we considered CFp and CFn separately, the statistical significance only remained in pan class="Gene">CFp, however IFN-γ and TNF-α results were also higher in γδ than in αβ from CFn (Fig 5).

The percentage of cytokine-producing cells, αβ or γδ-positive, in total T lymphocytic population was calculated (Fig 6). Both subsets contributed to the same extent in the percentage of IFN-γ and TNF-α-positive lymphocytes. In contrast, the highest number of IL-2-producing lymphocytes always proceeded from the αβ subset. Again, we did not find significant differences between groups.

Figure 6

Percentage of intracytoplasmic cytokine-producing αβ T cells (top) and γδ T cells (bottom) within total T lymphocytes after 10 days of culture with cytosolic extract from Intracytoplasmic cytokine expression was detected, by three color cytometry, in 10000 gated T lymphocytes. Column values correspond to mean, bar values correspond to standard error of the mean. Significant differences were not found between groups (ANOVA). p values were obtained from means comparison between αβ and γδ T lymphocytes within each group: controls (n = 17), Cystic fibrosis patients infected by PA (CFp, n = 9) and Cystic fibrosis patients not infected by PA (CFn, n = 4) (Student t test for paired samples).

Percentage of intracytoplasmic cytokine-producing αβ T cells (top) and γδ T cells (bottom) within total T lymphocytes after 10 days of culture with cytosolic extract from Intracytoplasmic cytokine expression was detected, by three color cytometry, in 10000 gated T lymphocytes. Column values correspond to mean, bar values correspond to standard error of the mean. Significant differences were not found between groups (ANOVA). p values were obtained from means comparison between αβ and γδ T lymphocytes within each group: controls (n = 17), Cystic fibrosis pan class="Species">patients infected by PA (CFp, n = 9) and Cystic fibrosis patients not infected by PA (CFn, n = 4) (Student t test for paired samples).

Correlation with clinical status

No differences were found in cytokine secretion, activation markers and PBMC proliferation in relation to clinical severity of pan class="Species">patients (data not shown).

Discussion

The present study is the first, to our knowledge, that determines the "in vitro" intracytoplasmic cytokine response to Pseudomonas aeruginosa (PA) in αβ and γδ T lymphocytes. We first expecies">panded PA-reactive T cells for 10 days and then we restimulated them with pan class="Chemical">PMA-Io. The cytokine-producing frequencies among αβ and γδ T cells were found in this order: TNF-α>IFN-γ>IL-2, for both subsets. Our results indicate that despite recognizing different antigens from PA [9], αβ and γδ T cells have a similar profile of cytokine secretion, but PAc stimulation induce more γδ than αβ IFN-γ and TNF-α-positive cells. αβ and γδ contribution to the percentage of IFN-γ and TNF-α-producing cells in total T lymphocytic population was the same although the αβ subset was always predominant.

Cytokine production by αβ and γδ T lymphocytes on stimulation with mycobacteria preparations and its purified phosphoantigens has been previosly studied. The secretion profile was limited to Th1-type cytokines [24,25,34-36]. One study compared cytokine levels in supernatants of αβ and γδ purified cells cultured with live Mycobacterium tuberculosis [25] and concluded that γδ T cells were more efficient producers of IFN-γ.

These and our present findings reinforce the evidence of an important role for γδ T lymphocytes in the response to bacteria through IFN-γ secretion [21]. Furthermore, an "in vivo" γδ T memory response, already suggested in humans [37] has been recently described in BCG-vaccinated macaques [26]. This opens the way to new immunization strategies.

On the other hand, our findings did not support the hypothesis that there is a bias in CF T lymphocytes function toward a Th2 response [17,23]. There are contradictory reports in this field. Agreement exists about the protective role of the cellular response to PA [15-17] but the kind of cytokines responsible for a good or a deleterious response in CF is still not elucidated. Some authors demonstrate a beneficial role of the inflammatory cytokine IFN-γ [17] and others implicate a defective production of pan class="Gene">IL-10 in the pulmonary lesions of CF patients [4]. Moss et al [38], found a lower IFN-γ secretion by CD4-positive T cells in CF patients but the stimulus (anti-CD3 plus PMA) and the tested subpopulation differed from ours.

In a previous work [8] we demonstrated a significant increase of peripheral blood γδ T lymphocytes in cystic fibrosis pan class="Species">patients. In later work we showed an "in vitro" preferent γδ T cells proliferation in response to small cytoplasmic phosphorilated non-peptidic compounds from PA, in healthy individuals [9]. Our present results show that the percentage of γδ-positive cells in total T lymphocytes increases to the same extent in healthy and CF individuals after PBMC culture with PAc. In both groups the expanded subset of γδ cells, was Vγ9+Vδ2+CD4-CD8-, already described as predominant in peripheral blood [39,40] and reactive to ubiquitous bacterial phosphorilated compounds [41,42]. In contrast, this subset was reported as not responsive to bacterial phosphoantigens in patients with active pulmonary tuberculosis in comparison to normal PPD+ subjects [14].

In the current study we have not found differences between controls and patients in pan class="Gene">CD25 and CD45RO expression by γδ T cells after stimulation with PA. Before culture, patients presented a higher percentage of γδ CD45RO-positive than controls, probably due to "in vivo" stimulation by PA or other microorganisms.

In contrast, CD25 and pan class="Gene">CD45RO expression by CF αβ T lymphocytes was lower than in controls. Selective apoptosis could account for this, but we can not exclude a concomitant low activation-induced expression. Proliferative response to PA was also lower in patients. Therefore, patients are more exposed to PA but they could present a lower percentage of αβ T lymphocytes specific to PA.

Intrinsic and PA-derived T cell defects have already been described in CF patients and in pan class="Species">mouse strains prone to chronic infection by PA [5,43]. They have been attributed to inhibitory factors produced by accessory cells or by PA. In this study no significant differences were found between PA-positive and PA-negative patients, although the present work has been mainly focused on intracytoplasmic cytokine production. In addition, patients with moderate and slight severity did not present differences in comparison to patients with good or excellent status. Therefore, Tαβ defects from CF individuals could be related to intrinsic characteristics or to inhibitory mediators produced by other cells.

γδ T cells have a crucial role in protecting airway function and integrity [6,7] but they have been also implicated in some pathogenic cytokine disregulation and development of airway inflammation [11]. Their cytokine production in response to bacterial products is tightly regulated and this regulation depends on contact with live bacteria [44]. We postulate that in CF pan class="Species">patients the persistent colonization by PA could avoid the IFN-γ and TNF-α switching-off that develops in acute infection, when the amount of live bacteria decreases.

Finally, this study has been done in T subsets from peripheral blood and further studies at pulmonary level will be needed to elucidate if CF epithelial cells are targets of an excessive inflammatory response mediated by γδ T lymphocytes.

Conclusion

We have demonstrated that γδ-positive T cells from peripheral blood are high "in-vitro" producers of IFN-γ and TNF-α cytokines in response to P. aeruginosa. They contribute at the same extent as the predominant αβ subset to the percentage of cytokine-positive cells in total T lymphocyte subpopulation. The only differences found in pan class="Disease">cystic fibrosis patients have been in the αβ activation markers expression and the PBMC proliferative response.

γδ T cells could play a crucial role in airway defense against P. aeruginosa and their persistent activation could contribute to the pan class="Disease">excessive lung inflammation in cystic fibrosis patients.

Abbreviations

BFA: Brefeldin-A

CF: Cystic Fibrosis

CFTR: Cystic Fibrosis Transmembrane Conductance Regulator

c.p.m.: counts per minute

FITC: Fluorescein isothiocyanate

Io: Ionomycine

MAbs: Monoclonal antibodies

PA: Pseudomonas aeruginosa

PAc: Heat treated cytosolic fraction from PA

PBMC: Peripheral blood mononuclear cells

PE: Phycoerytrin

PerCP: Peridin-chlorophyl-A-protein

PHA: Phytohemaglutinin

PMA: Phorbol 12-Myristate 13-Acetate

SC: Schwachman score

SI: Stimulation index