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1.
Braz. oral res. (Online) ; 32: e120, 2018. tab, graf
Article in English | LILACS | ID: biblio-974436

ABSTRACT

Abstract The present study aims to evaluate the longitudinal effects of induced experimental infections in gnotoxenic animals on the expression of inflammatory chemokines and their receptors in periradicular tissues. The null hypothesis tested was that Enterococcus faecalis and Fusobacterium nucleatum had no effect on CCR5, CCL5, CXCL10, CCL2/MCP-1, CXCR2 and CCR1 expression. Two groups of five animals (n = 5) aged between 8 and 12 weeks were used in this study. The animals were anaesthetized, and coronary access was performed in the first molar on the right and left sides. Microorganisms were inoculated into the left molar, and the right molar was sealed without contamination to function as a control. Animals were sacrificed 7 and 14 days after infection, and periapical tissues were collected. The cytokine mRNA expression levels were assessed using real-time PCR. The chemokine mRNA expression levels demonstrated that the experimental infection was capable of inducing increased chemokine expression on day 7 compared to that on day 14, except for CCR5 and CCL5, which showed no changes. The gnotoxenic animal model proved to be effective and allowed evaluation of the immune response against a known infection. Additionally, this study demonstrates that gene expression of chemokines and their receptors against the experimental infection preferentially prevailed during the initial phase of induction of the periradicular alteration (i.e., on day 7 post-infection).


Subject(s)
Animals , Mice , Gram-Positive Bacterial Infections/immunology , Chemokines/analysis , Receptors, Chemokine/analysis , Dental Pulp Cavity/immunology , Dental Pulp Diseases/immunology , Fusobacterium Infections/immunology , Germ-Free Life , Periapical Diseases/immunology , Periapical Diseases/microbiology , Reference Values , Time Factors , Gene Expression , Chemokines/genetics , Receptors, Chemokine/genetics , Dental Pulp Cavity/microbiology , Dental Pulp Diseases/microbiology , Real-Time Polymerase Chain Reaction
2.
Einstein (Säo Paulo) ; 14(3): 391-397, July-Sept. 2016. tab, graf
Article in English | LILACS | ID: lil-796967

ABSTRACT

ABSTRACT Objective: To evaluate growth factors and cytokines in samples of platelet-rich plasma obtained by three different centrifugation methods. Methods: Peripheral blood of six individuals with no hematological diseases, aged 18 to 68 years, was drawn to obtain platelet-rich plasma, using the open method and commercial columns by Medtronic and Biomet. The products obtained with the different types of centrifugation were submitted to laboratory analysis, including pro-inflammatory cytokines and chemokines by flow cytometry assays, the concentration of fibroblast growth factors-2 (FGF-2) and transforming growth factor-beta1 (TGF-β1). Results: The diverse separation methods generated systematically different profiles regarding number of platelets and leukocytes. The Medtronic system yielded a product with the highest concentration of platelets, and the open method, with the lowest concentration of platelets. The results of cytokine analysis showed that the different types of centrifugation yielded products with high concentrations of interleukin 8, interleukin 1β. The open system resulted in a product with high levels of interleukin 6. Other cytokines and chemokines measured were similar between systems. The product obtained with the open method showed higher levels of TGF-β1 in relation to other systems and low FGF-2 levels. Conclusion: The formed elements, growth factors and cytokines in samples of platelet-rich plasma varied according to the centrifugation technique used.


RESUMO Objetivo: Avaliar fatores de crescimento e citocinas em amostras de plasma rico em plaquetas obtidas por três diferentes métodos de centrifugação. Métodos: Foi coletado sangue periférico de seis indivíduos, sem doença hematológica, com idades entre 18 e 68 anos, para obtenção de plasma rico em plaquetas, utilizando o método aberto e sistemas comerciais das empresas Medtronic e Biomet. Os produtos obtidos com os diferentes tipos de centrifugação foram submetidos às análises laboratoriais, incluindo citocinas próinflamatórias e quimiocinas, por meio de ensaios de citometria de fluxo, concentração do fator de crescimento fibroblástico-2 (FGF-2) e fator de crescimento transformador-beta1 (TGF-β1). Resultados: As diferentes centrifugações geraram perfis sistematicamente diferentes referentes ao número de plaquetas e de leucócitos. O sistema da Medtronic originou produto com a maior concentração de plaquetas, e o método aberto com a menor concentração de plaquetas. Os resultados da análise de citocinas demonstraram que os diferentes tipos de centrifugação originaram produtos com elevadas concentrações de interleucina 8 e interleucina 1β. O sistema aberto resultou em produto com elevados níveis de interleucina 6. As demais citocinas e quimiocinas mensuradas foram similares entre os sistemas. O produto obtido com o método aberto apresentou níveis superiores de TGF-β1 em relação aos demais sistemas e reduzidos níveis de FGF-2. Conclusão: Os elementos figurados, fatores de crescimento e citocinas, em amostras de plasma rico em plaquetas, variaram conforme a técnica de centrifugação utilizada.


Subject(s)
Humans , Adolescent , Adult , Middle Aged , Aged , Young Adult , Cytokines/analysis , Intercellular Signaling Peptides and Proteins/analysis , Platelet-Rich Plasma/chemistry , Centrifugation/methods , Cytokines/blood , Interleukins/analysis , Interleukins/blood , Chemokines/analysis , Chemokines/blood , Intercellular Signaling Peptides and Proteins/blood , Rotator Cuff Injuries/surgery
3.
Bauru; s.n; 2016. 127 p. tab, ilus, graf.
Thesis in Portuguese | LILACS, BBO | ID: biblio-882111

ABSTRACT

O Sistema renina-angiotensina (SRA) tem sido relatado como um importante modulador de processos inflamatórios e imunológicos, incluindo a doença periodontal (DP). Estudos sugerem neste sistema um eixo alternativo (ECA-2 /ANG(1-7) /MAS) que atuaria como um contra-regulador de efeitos mediados pelo clássico eixo (ECA /ANGII /AT1). Sabe-se que bactérias periodontopatogênicas, como a Porphyromonas gingivalis (Pg), possuem componentes bioativos de membrana (ex. lipopolissacarídeos-LPS) capazes de induzir uma forte resposta imune no hospedeiro devido à liberação de citocinas nas células, entre elas Interleucina (IL)- 1ß. Neste contexto, fibroblastos são as células mais abundantes nos tecidos periodontais e possuem em sua superfície celular receptores necessários para o reconhecimento da invasão bacteriana, ativando cascatas intracelulares, que levam à produção de citocinas. O objetivo deste estudo foi verificar se os eixos ECA/ ANGII/ AT1 e ECA-2/ ANG(1-7)/ MAS contribuem para a produção e/ ou regulação de citocinas inflamatórias (CI) por fibroblastos de gengiva humana (HGF) e ligamento periodontal humano (HPLF) estimulados por IL-1ß. Após o pré-tratamento com Losartan e Ang (1-7) ou silenciamento mediado por RNA de interferência (RNAi) de AT1, HGF e HPLF foram estimulados por IL-1ß por 3 horas (RNAm) ou 24 horas (proteína). Expressão de RNAm para AT1, MAS, ECA, ECA-2, IL-1ß, TNF-α, IL-6, IL-8, IL-10, TGF-ß, CXCL12, RANK-L e OPG foram avaliados por RT-qPCR e das proteínas IL-6, IL-8, ECA e ECA-2 por ELISA. Foi realizado também Western Blot para detecção de AT1 e ECA nos extratos celulares e dosagem de nitrito no sobrenadante das culturas. Ambos os subtipos de fibroblastos mostraram aumento da expressão de RNAm para AT1, IL-1ß, IL-6, IL-8, TNF-α e OPG, quando estimulados por IL-1ß. No entanto, apenas em HPLF foi observado aumento para MAS, ECA e TGF-ß. Losartan e Ang (1-7) não modularam o transcrito, a secreção de CI e nem a produção de nitrito no sobrenadante das culturas, tanto em HGF como em HPLF. O silenciamento do receptor AT1 reduziu a secreção de IL-6 e IL-8 induzida por IL-1ß em cultura de HGF e HPLF e aumentou a expressão gênica de OPG somente em HGF. Estes resultados sugerem que o silenciamento de AT1, mas não o bloqueio farmacológico deste receptor pelo antagonista Losartan, em HGF e HPLF, pode controlar a produção de IL-6 e IL-8, que por sua vez contribuem para a patogênese periodontal.(AU)


The renin-angiotensin system (RAS) has been reported as an important modulator of inflammatory and immune responses, including periodontal disease (PD). Studies suggest an alternative axis as part of this system (ACE-2 / ANG (1-7) / MAS) that would act as counter-regulatory to the classical axis (ECA / ANGII / AT1). It is known that periodontal bacteria such as Porphyromonas gingivalis (Pg) have bioactive components in their membrane (such as lipopolysaccharide-LPS) capable of inducing a strong immune response in the host due to the release of cytokines in cells, including interleukin (IL) - 1ß. In this regard, fibroblasts are the most abundant cells in periodontal tissues and receptors needed for the recognition of bacterial invasion by activating intracellular cascades that lead to cytokine production. The aim of this study was to determine whether the axes ACE / ANGII / AT1 and ACE-2 / ANG (1-7) / MAS contribute to the production and / or regulation of inflammatory cytokines (IC) by fibroblasts of human gingiva (HGF) and human periodontal ligament (HPLF) stimulated IL-1ß. After pre-treatment with Losartan, Ang (1-7) or silencing mediated by RNA interference (RNAi) of AT1, HGF and HPLF were stimulated by IL-1ß for 3 hours (RNAm) or 24 hours (protein). Expression mRNA for AT1, MAS, ACE, ACE-2, IL-1ß, TNF-α, IL-6, IL-8, IL-10, TGF-ß, CXCL12, RANK-L and OPG was assessed by RT- qPCR and proteins IL-6, IL-8, ACE and ACE-2 by ELISA. Western Blot for the detection of AT1 and ECA and dosage of nitrite was also performed. Experiments stimulated by IL-1ß showed a positive control for gene expression AT1, IL-1ß, IL-6, IL-8, TNF-α and OPG in HGF and HPLF and MAS, ACE and TGF-ß only HPLF. Losartan and Ang (1-7) did not modulate the transcription and secretion of IC and no nitrite production in the culture supernatant of HGF and HPLF. The silencing AT1 reduced IL-6 secretion and IL-8 induced by IL- ß in cultured HGF and HPLF and increased OPG gene expression only HGF. These results suggest that silencing AT1, but not pharmacological blockade of this receptor by Losartan in HPLF and HGF, can control the production of IL-6 and IL-8, which in turn contribute to the pathogenesis of periodontal disease.(AU)


Subject(s)
Humans , Chemokines/metabolism , Cytokines/metabolism , Fibroblasts/physiology , Interleukin-1beta/physiology , Renin-Angiotensin System/physiology , Analysis of Variance , Angiotensin II Type 1 Receptor Blockers/pharmacology , Angiotensin II/analysis , Angiotensin II/physiology , Angiotensin I/analysis , Angiotensin I/physiology , Blotting, Western , Cells, Cultured , Chemokines/analysis , Cytokines/analysis , Gingiva/cytology , Losartan/pharmacology , Peptide Fragments/analysis , Peptide Fragments/physiology , Peptidyl-Dipeptidase A/analysis , Peptidyl-Dipeptidase A/physiology , Periodontal Ligament/cytology , Polymerase Chain Reaction , Proto-Oncogene Proteins/analysis , Proto-Oncogene Proteins/physiology , Receptor, Angiotensin, Type 1/analysis , Receptor, Angiotensin, Type 1/physiology
4.
Salvador; s.n; 2014. 111 p. ilus, tab.
Thesis in Portuguese | LILACS | ID: biblio-1000937

ABSTRACT

A hanseníase ou mal de Hansen (MH), causada pelo patógeno Mycobacterium leprae, ainda constitui um problema de saúde pública no Brasil, e em especial no Maranhão. A doença é hiperendêmica em 77 municípios do Estado. A resposta imune ao patógeno de indivíduos dessas regiões permanece obscuro podendo contribuir na manutenção da hiperendemia. Por isso, este estudo teve por objetivo caracterizar o perfil clínico-epidemiológico e imunológico de pacientes infectados por M. leprae, e de seus contatos, procedentes de área hiperendêmica. Para o desenvolvimento deste trabalho foi realizado um estudo transversal foi realizado nos municípios de Açailândia, Imperatriz e São Luís, no período 2009 a 2012. Pacientes e contatos foram clinicamente avaliados e tiveram os dados epidemiológicos coletados. Uma amostra de sangue foi obtida para realização das sorologias para detecção de anticorpos IgM anti-PGL1 pelos testes de ELISA e ML-Flow, e dosagem de citocinas e quimiocinas. A análise descritiva demonstrou que a maioria dos pacientes eram adultos, do gênero masculino, diagnosticados principalmente com as formas intermediárias da doença (60%)...


Leprosy, caused by the pathogen Mycobacterium leprae, it is a public health problem in Brazil yet, especially in Maranhão. The disease is hyperendemic in 77 counties of the State. Immune response to the pathogen of individuals in these regions remains unclear and may be contributing to maintenance of high endemicity. Therefore, this study aimed to characterize epidemiological and immunological profile of patients infected with M. leprae, and their contacts, from hyperendemic regions. Cross-sectional study was accomplished in Açailândia, Imperatriz and São Luís counties, 2009-2012. Patients and contacts were clinically evaluated and had their epidemiological data collected. A blood sample was obtained for performing serological tests IgM anti-PGL1 detection by ELISA and ML-Flow and measurement of cytokines and chemokines. Descriptive analysis showed that most patients were adults, male, diagnosed with intermediate forms mainly (60%)...


Subject(s)
Adult , Cytokines/analysis , Cytokines/blood , Epidemiology/statistics & numerical data , Leprosy/transmission , Chemokines , Chemokines/analysis , Chemokines/blood , Chemokines/chemical synthesis , Serology/statistics & numerical data , Serology/methods
5.
Belo Horizonte; s.n; 2014. 159 p. ilus, tab.
Thesis in Portuguese | LILACS, BBO | ID: lil-715980

ABSTRACT

A periodontite crônica (PC) é a principal forma de doença periodontal destrutiva e resulta da interação entre bactérias e resposta inflamatória do hospedeiro, podendo ser afetada por fatores ambientais como o fumo. o objetivo do estudo foi avaliar a expressão de citocinas e quimiocinas, assim como a densidade de células dendríticas (CDs) imaturas e maduras, e densidade do infiltrado inflamatório no tecido gengival de indivíduos não-fumantes (NF) e fumantes (F), diagnosticados com periodontite crônica. O estudo foi aprovado pelo COEP-UFMG (423/11) e foram recrutados 24 indivíduos NF e 21 F...


Subject(s)
Humans , Male , Female , Cytokines/analysis , Smoking/adverse effects , Chronic Periodontitis/complications , Chemokines/analysis , Dendritic Cells/classification
6.
J. bras. nefrol ; 31(4): 286-296, out.-dez. 2009. tab
Article in Portuguese | LILACS | ID: lil-549915

ABSTRACT

O transplante renal é a melhor modalidade de terapia renal substitutiva até o momento. Infelizmente a sobrevida do enxerto é interrompida pelos episódios de rejeição aguda ou mesmo de fibrose intersticial atrofia tubular. A dosagem de quimiocinas e citrocinas urinárias como ferramenta alternativa para o diagnóstico dessas complicações tem sido relatada nos últimos anos. Estas substâncias estão sabidamente relacionadas com os mecanismos imunoinflamatórios do transplante renal podendo ser detectadas no tecido renal no plasma e na urina de pacientes transplantados. Drogas anti-inflamatórias inibidores do sistema renina angiotensina e alguns antagonistas de receptores de citocinas ainda utilizados em nível experimental podem interferir com a expressão desses mediadores do sistema imune e por conseguinte alterar a evolução do transplante renal. Neste sentido pretende-se neste artigo fazer uma revisão dos estudos sobre a mensuração de citocinas quimiocinas e dos seus receptores na urina no plasma e no tecido renal de pacientes transplantados no intuito de avaliar uma possível associação entre os níveis desses mediadores e as complicações do transplante renal e sobrevida do enxerto.


Renal transplantation is the best modality of renal replacement therapy so far. Unfortunately, graft survival is interrupted by episodes of acute rejection or tubular atrophy of interstitial fibrosis. The measurement of urinary chemokines and citrocinas as an alternative tool for the diagnosis of these complications have been reported in recent years. These substances are known to be related to immunoinflammatory mechanisms of renal transplantation can be detected in renal tissue in plasma and urine of transplant patients. Anti-inflammatory drugs inhibiting the renin angiotensin receptor antagonists and some cytokines also used on an experimental level can interfere with the expression of these mediators of the immune system and thus alter the course of renal transplantation. In this sense we intend to make this article a review of studies on the measurement of cytokines chemokines and their receptors in the plasma and urine in the renal tissue of patients transplanted in order to evaluate a possible association between the levels of these mediators and the complications of the transplant and renal graft survival.


Subject(s)
Humans , Male , Female , Cytokines/analysis , Cytokines/biosynthesis , Chemokines/analysis , Chemokines/biosynthesis , Graft Rejection/diagnosis , Kidney Transplantation/adverse effects , Kidney Transplantation/physiology
7.
Journal of Korean Medical Science ; : 775-781, 2009.
Article in English | WPRIM | ID: wpr-153148

ABSTRACT

Dominant inflammatory cytokines might be different depending on the underlying causes of acute lung injury (ALI). The role of kertinocyte-derived chemokine (KC), a potent chemoattractant for neutrophils, has not been clearly established in hemorrhage-induced ALI. In this study, lung injury and cytokine expressison were evaluated in LPS- or hemorrhage-induced ALI models of BALB/c mice. The myeloperoxidase activities at 4 hr after hemorrhage and LPS-injection were 47.4+/-13.0 and 56.5+/-16.4 U/g, respectively. NF-kappa B activity peaked at 4 hr after hemorrhage, which was suppressed to the control level by anti-high mobility group B1 (HMGB1) antibody. Lung expressions of TNF-alpha, MIP-2, and IL-1beta were increased by LPS injection. However, there was only a minimal increase in IL-1beta and no expressions of TNF-alpha or MIP-2 in hemorrhage-induced ALI. In contrast, lung KC increased significantly at 4 hr after hemorrhage compared to control levels (83.1+/-12.3 vs. 14.2+/-1.6 pg/mL/mg by ELISA) (P<0.05). By immunohistochemical staining, lung neutrophils stained positive for KC. Increased KC was also observed in bronchoalveolar lavage fluid and plasma. KC plays an important role in hemorrhage-induced ALI.


Subject(s)
Animals , Humans , Mice , Acute Lung Injury/etiology , Antibodies/immunology , Chemokine CXCL2/analysis , Chemokines/analysis , Chickens , HMGB1 Protein/metabolism , Interleukin-1beta/analysis , Lipopolysaccharides/toxicity , Mice, Inbred BALB C , NF-kappa B/metabolism , Neutrophils/immunology , Peroxidase/analysis , Shock, Hemorrhagic/complications , Time Factors , Tumor Necrosis Factor-alpha/analysis
8.
Saudi Medical Journal. 2008; 29 (8): 1088-1094
in English | IMEMR | ID: emr-94299

ABSTRACT

To investigate the effect of melatonin on the colon inflammatory injury of rats with colitis and determine whether this effect is associated with inhibition of chemoattractant molecules interleukin [IL-8] and monocyte chemoattractant protein [MCP-1]. The study was designed and implemented in JingMen No.1 People's Hospital, HuBei Province, from May 2006 to April 2007. It involved 72 animals divided into 6 groups of 12 each: normal group, model group, 5-aminosalisalicylic acid group,and melatonin group [dose of 2.5, 5.0, and 10.0mg/kg]. Rat colitis model was established by 2, 4, 6-trinitrobenzene sulfonic acid [TNBS] enema. Interlukin-8 and MCP-1 proteins in colon tissue were examined by immunohistochemistry and western blot. The messenger-RNA expressions of chemokines were determined by reverse transcription polymerase chain reaction analysis. Trinitrobenzene sulfonic acid enema resulted in pronounced pathological changes of colonic mucosa in model rats, which were in accordance with the significantly elevated myeloperoxidase activity. Expressions of chemokines were up-regulated in colitis. Melatonin treatment reduced colonic lesions and improved colitis symptom, and decreased the protein and mRNA expressions of IL-8 and MCP-1 significantly in colon tissues of rats with colitis. Chemokines IL-8 and MCP-1 are elevated in mucosal tissues in colitis and play an important role in the perpetuation of tissue destructive inflammatory processes; melatonin reduces colonic inflammatory injury of rats colitis through down-regulating the expressions of chemokines. Melatonin can be considered as a novel therapeutic alternative for the treatment of inflammatory bowel disease


Subject(s)
Male , Female , Animals, Laboratory , Melatonin , Chemokines/analysis , Colitis/metabolism , Colitis/chemically induced , Colitis/drug therapy , Disease Models, Animal , Rats , Trinitrobenzenesulfonic Acid
9.
Journal of Korean Medical Science ; : 37-42, 2007.
Article in English | WPRIM | ID: wpr-226408

ABSTRACT

Bronchiolitis is a risk factor for the development of childhood asthma. Eosinophilic inflammation in airways plays an important role in the pathophysiology of both bronchiolitis and asthma. To investigate this inflammation, we measured the eosinophil cationic protein (ECP), regulated on activation normal T-cell expressed and secreted (RANTES) and eotaxin levels in nasopharyngeal secretions (NPS). Twenty-eight patients with RSV bronchiolitis (RSV group), 11 patients with non-RSV bronchiolitis (non-RSV group) and 7 controls were enrolled in this study. ECP, RANTES, and eotaxin levels were measured by enzyme immunoassays. The ECP level in the NPS of the RSV group was significantly higher than that in the NPS of the non-RSV group and controls. RANTES and eotaxin levels in infants with bronchiolitis were significantly higher than those in the controls, but there was no significant difference between the RSV and non-RSV groups. In conclusion, with regard to eosinophilic airway inflammation, as compared with non-RSV bronchiolitis, RSV bronchiolitis may be more similar to childhood asthma.


Subject(s)
Male , Infant , Humans , Female , Respiratory Syncytial Virus Infections/immunology , Chemokine CCL5/analysis , Nasopharynx/immunology , Eosinophil Cationic Protein/analysis , Chemokines, CC/analysis , Chemokines/analysis , Bronchiolitis/immunology
10.
Braz. j. med. biol. res ; 38(9): 1359-1365, Sept. 2005. tab
Article in English | LILACS | ID: lil-408363

ABSTRACT

Asthma and chronic obstructive pulmonary disease (COPD) are common respiratory illnesses characterized by chronic inflammation of the airways. The characterization of induced or spontaneously produced sputum is a useful technique to assess airway inflammation. In the present study, we compared the concentrations of CCL2, CCL11, CXCL8, and tumor necrosis factor-alpha (TNF-alpha) in plasma and induced sputum of patients with severe asthma or COPD and correlated the levels of these mediators with inflammatory cells in sputum. Asthmatic patients had elevated levels of eosinophils (40.1 ± 6.24 percent) in sputum whereas neutrophils (63.3 ± 4.66 percent) predominated in COPD patients. The levels of the chemokine CCL11 were markedly increased in sputum (708.7 ± 330.7 pg/ml) and plasma (716.6 ± 162.2 pg/ml) of asthmatic patients and correlated with the percentage of eosinophils in induced sputum. The concentrations of CXCL8 (817.0 ± 105.2 pg/ml) and TNF-alpha (308.8 ± 96.1 pg/ml) were higher in sputum of COPD patients and correlated with the percentage of neutrophils in induced sputum. There was also an increase in the concentrations of CXCL8 (43.2 ± 6.8 pg/ml) in sputum of asthmatic patients. These results validate that sputum is a suitable method to assess chemokines and cytokines associated with asthma and COPD. Moreover, the mechanisms involved in the synthesis of CCL11 and CXCL8/TNF-alpha would be helpful to better understand the inflammatory profile associated with asthma and COPD, respectively.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Asthma/metabolism , Chemokines/analysis , Pulmonary Disease, Chronic Obstructive/metabolism , Sputum/chemistry , Tumor Necrosis Factor-alpha/analysis , Analysis of Variance , Asthma/blood , Biomarkers/analysis , Biomarkers/blood , Case-Control Studies , Pulmonary Disease, Chronic Obstructive/blood , Pulmonary Disease, Chronic Obstructive/immunology
11.
Rev. patol. trop ; 27(1): 1-10, jan.-jun. 1998. ilus
Article in Portuguese | LILACS | ID: lil-228004

ABSTRACT

Esta revisäo aborda recentes descobertas dque esclareceram a natureza das moléculas acessórias obrigatoriamente utilizadas pelo HIV para infectar células humanas, elucidando mecanismos de resistência à infecçäo e abrindo perspectivas de novos alvos para drogas e vacinas. Um ano após a descoberta do HIV, a molécula CD4 foi identificada como receptor primário utilizado no processo de infecçäo dos linfócitos T. Entretanto, há mais de uma década se sabia que só esta molécula näo era suficiente e que o HIV precisava de moléculas adicionais, ou co-receptores, para permitir a infecçäo da célula-alvo. Em 1996, vários grupos de pesquisa descobriram que receptores para citocinas, das quais bem caracterizadas...


Subject(s)
Humans , Receptors, HIV , HIV-1/chemistry , Chemokines/analysis , Acquired Immunodeficiency Syndrome/epidemiology , Acquired Immunodeficiency Syndrome/therapy
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