Cytokine synthesis by intestinal intraepithelial lymphocytes. Both gamma/delta T cell receptor-positive and alpha/beta T cell receptor-positive T cells in the G1 phase of cell cycle produce IFN-gamma and IL-5

Murine intestinal intraepithelial lymphocytes (IEL) have been shown to contain subsets of alpha/beta TCR+ and gamma/delta TCR+ T cells that spontaneously produce cytokines such as IFN-gamma and IL-5. We have now determined the nature and cell cycle stage of these cytokine-producing T lymphocytes in EIL by using IFN-gamma- and IL-5-specific ELISPOT assay, cytokine-specific mRNA-cDNA dot-blot hybridization and polymerase chain reaction, and flow cytometry (FACS) for DNA analysis. When CD3+ T cells from IEL of normal C3H/HeN mice were separated into low and high density fractions by discontinuous Percoll gradients, IFN-gamma and IL-5 spot-forming cells were only found in the former population. Analysis of mRNA for these cytokines by both IFN-gamma- and IL-5-specific dot-blot hybridization and polymerase chain reaction revealed that higher levels of message for IFN-gamma and IL-5 were also seen in the low density fraction. However, cell cycle analysis of these two fractions by FACS using propidium iodide showed a similar pattern of cell cycle stages in both low and high density populations (G0 + G1 approximately 96 to 98% and S/G2 + M approximately 2 to 4%). Finally, mRNA from gamma/delta TCR+ and alpha/beta TCR+ T cells in both low and high density fractions of IEL were analyzed for IFN-gamma and IL-5 message by polymerase chain reaction. After 35 cycles of amplification, both gamma/delta TCR+ and alpha/beta TCR+ T cells in the low density fraction expressed higher levels of message for these two cytokines when compared with the high density population. These results have now shown that both gamma/delta and alpha/beta TCR+ IEL can be separated into low and high density subsets and both fractions possess a similar stage of cell cycle. However, only the low density cells (in G1 phase) of both gamma/delta and alpha/beta TCR types possess increased cytokine-specific mRNA and produce the cytokines IFN-gamma and IL-5. Our results suggest that alpha/beta TCR+ and gamma/delta TCR+ IEL can produce cytokines without cell proliferation.

IL-2, IL-5, TNF-α and IFN-γ mRNA expression in epidermal keratinocytes of systemic lupus erythematosus skin lesions

OBJECTIVE: To analyze cytokine gene expression in keratinocytes from patients with systemic lupus erythematosus (SLE). INTRODUCTION: Keratinocytes represent 95% of epidermal cells and can secrete several cytokines. METHODS: Keratinocytes were obtained by laser microdissection from 21 patients with SLE (10 discoid and 11 acute lesions) at involved and uninvolved sites. All patients were receiving a low/moderate prednisone dose and 18 were receiving chloroquine diphosphate. IL-2, IL-5, TNF-α and IFN-γ gene expression was evaluated by real-time PCR and expressed as the ratio (R) to a pool of skin samples from 12 healthy volunteers. RESULTS: Heterogeneity in cytokine gene expression was found among patients with SLE. Eighteen of 38 valid SLE samples (47%) presented overexpression (R>1) of at least one cytokine. Lesional skin samples tended to show higher cytokine expression than samples from uninvolved skin (p = 0.06). IL-5 and IFN-γ were the most commonly overexpressed cytokines. Samples with cytokine overexpression corresponded to more extensive and severe lesions. Prednisone dose did not differ between samples without cytokine overexpression (15.71±3.45 mg/day) and those with overexpressed cytokines (12.68±5.41 mg/day) (p = 0.216). Samples from all patients not receiving diphosphate chloroquine had at least one overexpressed cytokine. CONCLUSIONS: The heterogeneous keratinocyte cytokine gene expression reflects the complex immunological and inflammatory background in SLE. Patients with severe/extensive skin lesions showed a higher frequency of cytokine gene overexpression. Increased IFN-γ and IL-5 expression suggests that Th1 and Th2 cells are involved in SLE skin inflammation. The possibility that prednisone and antimalarial drugs may have contributed to low cytokine gene expression in some samples cannot be ruled out.

IL-5 and IL-17A are critical for the chronic IgE response and differentiation of long-lived antibody-secreting cells in inflamed tissues

Prolonged survival of long-lived antibody-secreting cells in the BM has been implicated as a key component of long-term humoral immunity. The current study was designed to uncover the extrinsic signals required for the generation and maintenance of ASC in several niches (peritoneum, spleen and bone-marrow). Our results show that protein mixture of the Thalassophryne nattereri venom induced a chronic Th2 humoral response that is characterized by splenic hyperplasia with GC formation and venom retention by follicular DCs. Retention of B1a in the BM were observed. In the late phase (120 d) of chronic venom-response the largest pool of ASC into the peritoneal cavity consisted of B220(neg)CD43(high) phenotype; the largest pool of ASC into spleen was constituted by B220 positive cells (B220(high) and B220(low)), whereas the largest pool of ASC into in the BM was constituted by the B220(high)CD43(low) phenotype; and finally, terminally differentiated cells (B220(neg)CD43(high)) were only maintained in the inflamed peritoneal cavity in late phase. After 120 d a sustained production of cytokines (KC, IL-5, TNF-alpha, IL-6, IL-17A and IL-23) and leukocytes recruitment (eosinophils, mast cells, and neutrophils) were induced. IL-5- and IL-17A-producing CD4+ CD44+ CD40L+ Ly6C+ effector memory T cells were also observed in peritoneal cavity. Finally, treatment of venom-mice with anti-IL-5- and anti-IL17A-neutralizing mAbs abolished the synthesis of specific IgE, without modifying the splenic hyperplasia or GC formation. In addition, IL-5 and IL-17A negatively regulated the expansion of B1a in peritoneal cavity and BM, and promoted the differentiation of these cells in spleen. And more, IL-5 and IL-17A are sufficient for the generation of ASC B220(neg) in the peritoneal cavity and negatively regulate the number of ASC B220(Pos), confirming that the hierarchical process of ASC differentiation triggered by venom needs the signal derived from IL-5 and IL-17A. (C) 2012 Elsevier Ltd. All rights reserved.

Drug-specific in vitro release of IL-2, IL-5, IL-13 and IFN-gamma in patients with delayed-type drug hypersensitivity

BACKGROUND: The most prevalent drug hypersensitivity reactions are T-cell mediated. The only established in vitro test for detecting T-cell sensitization to drugs is the lymphocyte transformation test, which is of limited practicability. To find an alternative in vitro method to detect drug-sensitized T cells, we screened the in vitro secretion of 17 cytokines/chemokines by peripheral blood mononuclear cells (PBMC) of patients with well-documented drug allergies, in order to identify the most promising cytokines/chemokines for detection of T-cell sensitization to drugs. METHODS: Peripheral blood mononuclear cell of 10 patients, five allergic to beta-lactams and five to sulfanilamides, and of five healthy controls were incubated for 3 days with the drug antigen. Cytokine concentrations were measured in the supernatants using commercially available 17-plex bead-based immunoassay kits. RESULTS: Among the 17 cytokines/chemokines analysed, interleukin-2 (IL-2), IL-5, IL-13 and interferon-gamma (IFN-gamma) secretion in response to the drugs were significantly increased in patients when compared with healthy controls. No difference in cytokine secretion patterns between sulfonamide- and beta-lactam-reactive PBMC could be observed. The secretion of other cytokines/chemokines showed a high variability among patients. CONCLUSION: The measurement of IL-2, IL-5, IL-13 or IFN-gamma or a combination thereof might be a useful in vitro tool for detection of T-cell sensitization to drugs. Secretion of these cytokines seems independent of the type of drug antigen and the phenotype of the drug reaction. A study including a higher number of patients and controls will be needed to determine the exact sensitivity and specificity of this test.

Proviral integration site for Moloney murine leukemia virus 1, but not phosphatidylinositol-3 kinase, is essential in the antiapoptotic signaling cascade initiated by IL-5 in eosinophils

BACKGROUND: Eosinophil differentiation, activation, and survival are largely regulated by IL-5. IL-5-mediated transmembrane signal transduction involves both Lyn-mitogen-activated protein kinases and Janus kinase 2-signal transducer and activator of transcription pathways. OBJECTIVE: We sought to determine whether additional signaling molecules/pathways are critically involved in IL-5-mediated eosinophil survival. METHODS: Eosinophil survival and apoptosis were measured in the presence and absence of IL-5 and defined pharmacologic inhibitors in vitro. The specific role of the serine/threonine kinase proviral integration site for Moloney murine leukemia virus (Pim) 1 was tested by using HIV-transactivator of transcription fusion proteins containing wild-type Pim-1 or a dominant-negative form of Pim-1. The expression of Pim-1 in eosinophils was analyzed by means of immunoblotting and immunofluorescence. RESULTS: Although pharmacologic inhibition of phosphatidylinositol-3 kinase (PI3K) by LY294002, wortmannin, or the selective PI3K p110delta isoform inhibitor IC87114 was successful in each case, only LY294002 blocked increased IL-5-mediated eosinophil survival. This suggested that LY294002 inhibited another kinase that is critically involved in this process in addition to PI3K. Indeed, Pim-1 was rapidly and strongly expressed in eosinophils after IL-5 stimulation in vitro and readily detected in eosinophils under inflammatory conditions in vivo. Moreover, by using specific protein transfer, we identified Pim-1 as a critical element in IL-5-mediated antiapoptotic signaling in eosinophils. CONCLUSIONS: Pim-1, but not PI3K, plays a major role in IL-5-mediated antiapoptotic signaling in eosinophils.

IL-4 and -5 prime human mast cells for different profiles of IgE-dependent cytokine production

Mast cells (MC) are stem cell factor-dependent tissue-based hematopoietic cells with substantial functional heterogeneity. Cord blood-derived human MC (hMC) express functional receptors for IL-5, and IL-5 mediates stem cell factor-dependent comitogenesis of hMC in vitro. Although IL-5 is not required for normal hMC development, we considered that it might prime hMC for their high-affinity Fc receptor for IgE (FcɛRI)-dependent generation of cytokines, as previously demonstrated for IL-4. Compared with hMC maintained in stem cell factor alone, hMC primed with IL-5 expressed 2- to 4-fold higher steady-state levels of TNF-α, IL-5, IL-13, macrophage inflammatory protein 1α, and granulocyte-macrophage colony-stimulating factor transcripts 2 h after FcɛRI crosslinking and secreted 2- to 5-fold greater quantities of the corresponding cytokines, except IL-13, at 6 h. Unlike IL-4, IL-5 priming did not enhance FcɛRI-dependent histamine release. Thus, IL-5 augments cytokine production by hMC by a mechanism distinct from that of IL-4 and with a different resultant profile of cytokine production. These observations suggest a potentially autocrine effect of IL-5 on hMC for amplification of allergic immune responses, in addition to its recognized paracrine effects on eosinophils, and implicate both IL-4 and IL-5 in the modulation of the hMC phenotype.

Critical role of interleukin 5 and eosinophils in concanavalin A-induced hepatitis in mice.

BACKGROUND & AIMS: Eosinophils are observed in several liver diseases, but their contribution in the pathogenesis of these disorders remains poorly investigated. Concanavalin A (Con A)-induced hepatitis is an experimental model of immune-mediated liver injury in which natural killer T (NKT) cells play a critical role through the production of interleukin (IL)-4 and the expression of Fas ligand (FasL). Because activated NKT cells also produce IL-5, a critical cytokine for eosinophil maturation and function, the role of IL-5 was investigated in this model. METHODS: IL-5-deficient mice, eosinophil depletion in wild-type (WT) mice, and NKT cell transfer from WT- or IL-5-deficient mice into NKT cell-deficient mice were used to assess the role of IL-5 and eosinophils. RESULTS: Liver eosinophil infiltrate and IL-5 production were observed after Con A challenge. Liver injury was dramatically reduced in IL-5-deficient or eosinophil-depleted mice. In addition, residual hepatitis observed in Fas-deficient mice was abolished after IL-5 neutralization. Finally, we showed that NKT cells constituted a critical source of IL-5. Indeed, transfer of WT NKT cells to mice lacking NKT cells restored liver injury, whereas transfer of IL-5-deficient NKT cells did not. CONCLUSIONS: These observations highlight the pathologic role of IL-5 and eosinophils in experimental immune-mediated hepatitis.

IL-33 attenuates the development of experimental autoimmune uveitis

Interleukin (IL)-33 is associated with several important immune-mediated disorders. However, its role in uveitis, an important eye inflammatory disease, is unknown. Here we investigated the function of IL-33 in the development of experimental autoimmune uveitis (EAU). IL-33 and IL-33 receptor (ST2) were expressed in murine retinal pigment epithelial (RPE) cells in culture, and IL-33 increased the expression of Il33 and Mcp1 mRNA in RPE cells. In situ, IL-33 was highly expressed in the inner nuclear cells of the retina of naïve mice, and its expression was elevated in EAU mice. ST2-deficient mice developed exacerbated EAU compared with WT mice, and administration of IL-33 to WT mice significantly reduced EAU severity. The attenuated EAU in IL-33-treated mice was accompanied by decreased frequency of IFN-γ(+) and IL-17(+) CD4(+) T cells and reduced IFN-γ and IL-17 production but with increased frequency of IL-5(+) and IL-4(+) CD4 T cells and IL-5 production in the draining lymph node and spleen. Macrophages from the IL-33-treated mice show a significantly higher polarization towards an alternatively-activated macrophage (M2) phenotype. Our results therefore demonstrate that the endogenous IL-33/ST2 pathway plays an important role in EAU, and suggest that IL-33 represents a potential option for treatment of uveitis.

PAS-1, a protein from Ascaris suum, modulates allergic inflammation via IL-10 and IFN-gamma, but not IL-12

Helminths and their products have a profound immunomodulatory effect upon the inductive and effector phases of inflammatory responses, including allergy. We have demonstrated that PAS-1, a protein isolated from Ascaris strum worms, has an inhibitory effect on lung allergic inflammation due to its ability to down-regulate eosinophilic inflammation, Th2 cytokine release and IgE antibody production. Here, we investigated the role of IL-12, IFN-gamma and IL-10 in the PAS-1-induced inhibitory mechanism using a murine model of asthma. Wild type C57BL/6, IL-12(-/-), IFN-gamma(-/-) and IL-10(-/-) mice were immunized with PAS-1 and/or OVA and challenged with the same antigens intranasally. The suppressive effect of PAS-I was demonstrated on the cellular influx into airways, with reduction of eosinophil number and eosinophil peroxidase activity in OVA + PAS-1-immunized wild type mice. This effect well correlated with a significant reduction in the levels of IL-4, IL-5, IL-13 and eotaxin in BAL fluid. Levels of IgE and IgG1 antibodies were also impaired in serum from these mice. The inhibitory activity of PAS-I was also observed in IL-12(-/-) mice, but not in IFN-gamma(-/-) and IL-10(-/-) animals. These data show that IFN-gamma and IL-10, but not IL-12, play an important role in the PAS-1 modulatory effect. (C) 2008 Elsevier Ltd. All rights reserved.

Expressão gênica de interferon-gama, fator de necrose tumoral alfa e interleucinas 2 e 5 no baço de gatos naturalmente infectados por Leishmania spp: Karina Yukie Hirata. -

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Leukocytes from wheezing infants release lower amounts of IL-12 and IFN-gamma compared to non-wheezing infants

Objective This study investigated environmental endotoxin exposure during early life, sensitization to aeroallergens, the production of cytokines by LPS-stimulated leukocytes, and the development of a wheezing phenotype in a prospective cohort of infants with high risk of developing allergic diseases. Materials and Methods Eighty-four infants were followed from birth until 30 months of age. We assessed endotoxin concentration in house dust of their homes during the first 6 months of life. At age 30 months they were clinically evaluated to determine the development of wheezing and other clinical events, were skin prick tested, and had blood samples collected for the evaluation of cytokine release by LPS-stimulated peripheral blood mononuclear cells (PBMC). Results The level of endotoxin exposure during early life was not associated with development of a wheezing phenotype. On the other hand a higher incidence of respiratory infections occurred among recurrent wheezing (RW) infants. PBMC from RW children exposed to higher levels of environmental endotoxin (above 50?EU/mg) released less Interleukin (IL)-12p70 and IFN-? compared to the non-RW group. TNF-a, IL-10, IL-4, IL-5, and IL17 production by LPS-stimulated PBMC from RW and non-RW children was equivalent in both groups of environmental endotoxin exposure. Conclusion In this prospective cohort of infants with high risk of developing allergic diseases we observed that RW and non-RW children were exposed to similar levels of endotoxin early in life. LPS-stimulated PBMC from RW infants exposed to higher levels of endotoxin released significantly less IL-12 and IFN-? compared to non-RW infants. Pediatr Pulmonol. 2012. 47:10541060. (C) 2012 Wiley Periodicals, Inc.

Il ruolo del teatro di Sa’d Allah Wannus nel panorama del mondo arabo contemporaneo

INTRODUZIONE. Presentazione della ricerca e del metedo seguito per realizzarla. CAPITOLO PRIMO. Il contesto storico, politico e sociale di riferimento. - Storia della Siria, - La Siria politica e il conflitto israelo-palestinese - La società siriana: multiculturalismo, tradizione, islam. - Teatro e letteratura in Siria, e nel Bilad AlSham. CAPITOLO SECONDO. I testi. Traduzione integrale di due opere teatrali di Sa’d Allah Wannus. Breve presentazione. - “ Riti di segni e trasformazioni.”, (tukus al-isharat wa-l-tahawwulat), 1994. Il dramma si svolge nella Damasco del XIX secolo, dove un affare di morale e buon costume è il punto di partenza per la metamorfosi dei suoi protagonisti, mettendo a nudo le riflessioni, i desideri più intimi, le contraddizioni e le angosce di una società in crisi. Interessante l’analisi delle figure femminili di questa piece, le loro scelte, il loro ruolo nella società e soprattutto la presa di coscienza delle loro posizioni. - “ I giorni ubriachi.” , (Alayyam Almakhmura), 1997. Il ritratto di una famiglia siriana degli anni trenta. Due genitori, quattro figli, e un nipote che a distanza di anni decide di ripercorrere e raccontarci le loro storie.Una madre che vive tormentata dal suo spettro e che decide di abbandonare la propria famiglia e i propri figli per seguire un altro uomo. Un padre che tiene con violenza le redini delle proprie relazioni, e che rifiuta l’occidente in tutte le sue forme per restare aggrappato alle proprie tradizioni. Un figlio che sceglie l’ordine e la carriera militare, e che, incapace di risolvere il suo rapporto di dipendenza dalla madre, e di risolvere il conflitto tra la legge e un affetto quasi morboso, sceglie di suicidarsi. Un figlio che sceglie la via della perdizione, delle droghe, del furto e degli affari illegali, e che va incontro al successo e alla ricchezza... CAPITOLO TERZO. Biografia di Sa’d Allah Wannus, presentazione delle sue opere principali. Sa’d Allah Wannus (1941 – 1997) è sicuramente uno dei principali protagonisti nell’ambito del teatro arabo contemporaneo. Scrittore, critico, drammaturgo, riformatore, uomo impegnato politicamente, e infine essere umano nella lotta tra la vita e la morte (muore a 56 anni per tumore, dopo un lungo periodo di degenza). Mio intento è quello di analizzare l’opera di quest’autore, attraverso i suoi numerosi scritti e piece teatrali (purtroppo al giorno d’oggi ancora quasi interamente non tradotte dall’arabo), fino ad arrivare, attraverso queste, ad una lettura della società araba contemporanea, e al ruolo che il teatro assume al suo interno. Vita e opere di Sa’ad Allah Wannus. Nasce in Siria nel 1941 in un piccolo villaggio vicino alla città di Tartous, sulla costa mediterranea. Dopo aver terminato gli studi superiori, nel 1959, parte per Il Cairo (Egitto), per studiare giornalismo e letteratura. Rientra a Damasco nel 1964, lavorando al tempo stesso come funzionario al ministero della cultura e come redattore o giornalista in alcune riviste e quotidiani siriani. Nel 1966 parte per Parigi, dove studierà con Jean-Louis Barrault, e dove farà la conoscenza delle tendenze del teatro contemporaneo. Ha l’occasione di incontrare scrittori e critici importanti come Jean Genet e Bernard Dort, nonché di conoscere le teorie sul teatro di Brech e di Piscator, dai quali sarà chiaramente influenzato. In questi anni, e soprattutto in seguito agli avvenimenti del Maggio 1968, si sviluppa in modo determinante la sua coscienza politica, e sono questi gli anni in cui compone alcune tra le sue piece più importanti, come: Serata di gala per il 5 giugno (haflat samar min ajl khamsa huzayran) nel 1968, L’elefante, oh re del tempo! (al-fil, ya malik al-zaman!) 1969, Le avventure della testa del Mamelucco Jaber (Meghamarat ra’s al-mamluk Jabiir) 1970, Una serata con Abu-Khalil al- Qabbani (Sahra ma’a Abi Khalil Al-Qabbani) 1972, Il re è il re (al-malik uwa al-malik) 1977. Parallelamente porta avanti una intensa attività artistica e intellettuale. Soggiorna di nuovo in Francia e a Weimar, per portare a termine la sua formazione teatrale, fonda il Festival di teatro di Damasco, traduce e mette in scena numerosi spettacoli, scrive e pubblica numerosi articoli e una importante serie di studi sul teatro, intitolata: Manifesto per un nuovo teatro arabo (bayanat limasrah ‘arabi jadid) (1970). Scrive in numerose riviste e giornali e fonda la rivista La vita teatrale (al-hayyat al-masrahiyya), del quale sarà capo redattore. La visita del presidente egiziano Anouar Sadat a Gerusalemme nel 1977 e gli accordi di Camp David l’anno seguente, lo gettano in una profonda depressione. E’ l’inizio di un lungo periodo di silenzio e di smarrimento. Ritornerà a scrivere solamente nel 1989, con l’inizio della prima Intifada palestinese, scrive allora una piece teatrale intitolata Lo stupro (al-ightisab), dove presenta un’analisi della struttura dell’elite al potere in Israele. Questo testo apre una nuova epoca creativa, durante la quale Wannus compone alcuni testi molto importanti, nonostante la malattia e il cancro che gli viene diagnosticato nel 1992. Tra questi le pieces Miniature storiche (munamnamat tarakhiyya), nel 1993, e Rituali per una metamorfosi (tukus al-isharat wa-l-tahawwulat), nel 1994 e A proposito della memoria e della morte (‘an al-dhakira wa-l-mawt) nel 1996, una sua ultima opera in cui sono raccolti dei racconti, drammi brevi e una lunga meditazione sulla malattia e la morte. Nel 1997 l’UNESCO gli chiede di redigere il messaggio per la Giornata Mondiale del Teatro, che si tiene ogni anno il 27 marzo. Nel 1997, poche settimane prima della sua scomparsa, realizza insieme ad Omar Almiralay il film documentario Il y a tant de choses a reconter, una intervista in cui Wannus parla della sua opera, e del conflitto Israelo-Palestinese. Muore a 56 anni, il 15 maggio 1997, per un’amara coincidenza proprio il giorno anniversario della creazione di Israele. Wannus drammaturgo engagè: l’importanza del conflitto israelo palestinese nella sua opera. Un’analisi dell’influenza e dell’importanza che le opere di Wannus hanno avuto nel seno della società araba, e soprattutto il suo impegno costante nell’uso del teatro come mezzo per la presa di coscienza del pubblico dei problemi della società contemporanea. Punto cardine dell’opera di Wannus, il conflitto israelo palestinese, e il tentativo costante in alcune sue opere di analizzarne le cause, le strutture, le parti, i giochi di potere. E’ il simbolo di tutta la generazione di Wannus, e delle successive. Analisi delle illusioni e dei miti che la società araba ripropone e che Wannus ha cercato più volte di mettere a nudo. La lotta contro le ipocrisie dei governi, e il tentativo di far prendere coscienza alla società araba del suo ruolo, e delle conseguenze delle sue azioni. L’individuo, la famiglia, la società ... il teatro. Distruggere le apparenze per mettere a nudo l’essere umano nella sua fragilità. CONCLUSIONI. APPENDICE: Intervista con Marie Elias BIBLIOGRAFIA.