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1.
Rev. bras. ginecol. obstet ; 43(9): 669-675, Sept. 2021. tab, graf
Article in English | LILACS | ID: biblio-1351771

ABSTRACT

Abstract Objective Preeclampsia (PE) is a pregnancy-specific syndrome characterized by abnormal levels of cytokines and angiogenic factors, playing a role in the disease development. The present study evaluated whether immunological markers are associated with the gestational age and with the disease severity in preeclamptic women. Methods Ninety-five women who developed PE were stratified for gestational age as preterm PE (< 37 weeks) and term PE (≥ 37 weeks of gestation) and compared for disease severity as well as plasma concentration of angiogenic factors and cytokines. The concentrations of placental growth factor (PlGF), vascular endothelial growth factor (VEGF), Fms-like soluble tyrosine kinase (sFlt-1) and soluble endoglin (sEng), as well as the cytokines, tumor necrosis factor-α (TNF-α) and interleukin 10 (IL-10), were determined by enzyme-linked immunosorbent assay (ELISA). Results The comparison between preeclamptic groups showed a higher percentage of severe cases in preterm PE (82.1%) than in term PE (35.9%). Similarly, the concentrations of TNF-α, sFlt-1, and sEng, as well as TNF-α/IL-10 and sFlt-1/PlGF ratios were significantly higher in the preterm PE group. In contrast, concentrations of PlGF, VEGF, and IL-10 were significantly lower in women with preterm PE. Negative correlations between TNF-α and IL-10 (r = 0.5232) and between PlGF and sFlt1 (r = 0.4158) were detected in the preterm PE. Conclusion In pregnant women with preterm PE, there is an imbalance between immunological markers, with the predominance of anti-angiogenic factors and TNF-α, associated with adverse maternal clinical outcomes.


Resumo Objetivo A pré-eclâmpsia (PE) é uma síndrome específica da gravidez caracterizada por níveis anormais de citocinas e fatores angiogênicos, que desempenham um papel no desenvolvimento da doença. Este estudo avaliou se os marcadores imunológicos estão associados à idade gestacional e à gravidade da doença em mulheres com pré-eclâmpsia. Métodos Noventa e cinco mulheres que desenvolveram PE foram estratificadas pela idade gestacional em PE pré-termo (< 37 semanas) e PE a termo (≥ 37 semanas de gestação) e comparadas quanto à gravidade da doença, bem como à concentração plasmática de fatores angiogênicos e citocinas. As concentrações de fator de crescimento placentário (PlGF), fator de crescimento endotelial vascular (VEGF), tirosina quinase solúvel semelhante a Fms (sFlt-1) e endoglina solúvel (sEng), bem como as citocinas, fator de necrose tumoral alfa (TNF- α) e interleucina 10 (IL-10), foram determinados porensaio de imunoabsorção enzimática (ELISA, na sigla em inglês). Resultados A comparação entre os grupos com pré-eclâmpsia mostrou maior porcentagem de casos graves em PE pré-termo (82,1%) do que em PE a termo (35,9%). Da mesma forma, as concentrações de TNF-α, sFlt-1 e sEng, bem como as razões TNF-α/IL-10 e sFlt-1/PlGF foram significativamente maiores no grupo de PE pré-termo. Em contraste, as concentrações de PlGF, VEGF e IL-10 foram significativamente menores em mulheres com PE pré-termo. Correlações negativas entre TNF-α e IL-10 (r = 0.5232) e entre PlGF e sFlt1 (r = 0.4158) foram detectadas no grupo de PE pré-termo. Conclusão Em gestantes com PE pré-termo, ocorre um desequilíbrio entre os marcadores imunológicos, com predomínio de fatores antiangiogênicos e TNF-α, associados a desfechos clínicos maternos adversos.


Subject(s)
Humans , Female , Pregnancy , Infant, Newborn , Infant , Pre-Eclampsia , Biomarkers , Antigens, CD , Cytokines , Receptors, Cell Surface , Vascular Endothelial Growth Factor Receptor-1 , Vascular Endothelial Growth Factor A , Angiogenesis Inducing Agents , Placenta Growth Factor
2.
Mem. Inst. Oswaldo Cruz ; 106(6): 735-741, Sept. 2011. ilus, tab
Article in English | LILACS | ID: lil-602058

ABSTRACT

Multinucleated giant cells (MGC) are cells present in characteristic granulomatous inflammation induced by intracellular infectious agents or foreign materials. The present study evaluated the modulatory effect of granulocyte macrophage colony-stimulating factor (GM-CSF) in association with other cytokines such as interferon-gamma (IFN-γ), tumour necrosis factor-alpha, interleukin (IL)-10 or transforming growth factor beta (TGF-β1) on the formation of MGC from human peripheral blood monocytes stimulated with Paracoccidioides brasiliensis antigen (PbAg). The generation of MGC was determined by fusion index (FI) and the fungicidal activity of these cells was evaluated after 4 h of MGC co-cultured with viable yeast cells of P. brasiliensis strain 18 (Pb18). The results showed that monocytes incubated with PbAg and GM-CSF plus IFN-γ had a significantly higher FI than in all the other cultures, while the addition of IL-10 or TGF-β1 had a suppressive effect on MGC generation. Monocytes incubated with both pro and anti-inflammatory cytokines had a higher induction of foreign body-type MGC rather than Langhans-type MGC. MGC stimulated with PbAg and GM-CSF in association with the other cytokines had increased fungicidal activity and the presence of GM-CSF also partially inhibited the suppressive effects of IL-10 and TGF-β1. Together, these results suggest that GM-CSF is a positive modulator of PbAg-stimulated MGC generation and on the fungicidal activity against Pb18.


Subject(s)
Adult , Humans , Middle Aged , Young Adult , Antigens, Fungal/pharmacology , Cytokines/immunology , Giant Cells/drug effects , Granulocyte-Macrophage Colony-Stimulating Factor/pharmacology , Monocytes/immunology , Paracoccidioides/drug effects , Cells, Cultured , Giant Cells/immunology , Paracoccidioides/immunology
3.
Rev. Inst. Med. Trop. Säo Paulo ; 47(5): 263-266, Sept.-Oct. 2005.
Article in English | LILACS | ID: lil-417084

ABSTRACT

Os mecanismos utilizados pelo Paracoccidioides brasiliensis para sobreviver em células fagocitárias ainda não estão elucidados. O metabolismo celular férrico é muito importante para o crescimento de inúmeros patógenos intracelulares cuja capacidade de se multiplicarem em fagócitos mononucleares é dependente da disponibilidade intracelular do íon ferro. Assim, o objetivo deste trabalho foi investigar o papel do ferro intracelular sobre a capacidade do P. brasiliensis sobreviver em monócitos humanos. O tratamento de monócitos com deferoxamina, uma droga quelante, diminuiu a sobrevivência de leveduras do fungo de forma dose-dependente. O efeito inibidor da deferoxamina sobre a sobrevivência do P. brasiliensis foi revertido por transferrina saturada com ferro (holotransferrina) mas não por transferrina insaturada (apotransferrina). Estes resultados sugerem que a sobrevivência do P. brasiliensis em monócitos humanos é dependente do íon ferro.


Subject(s)
Humans , Apoproteins/pharmacology , Deferoxamine/pharmacology , Monocytes/microbiology , Paracoccidioides/drug effects , Siderophores/pharmacology , Transferrin/pharmacology , Deferoxamine/antagonists & inhibitors , Iron/physiology , Paracoccidioides/physiology , Siderophores/antagonists & inhibitors
6.
Rev. Inst. Med. Trop. Säo Paulo ; 41(4): 215-9, July-Aug. 1999.
Article in English | LILACS | ID: lil-246828

ABSTRACT

Kala-azar is the visceral form of leishmaniasis and it is caused by intracellular parasites from the complex Leishmania donovani. Golden hamster (Mesocricetus auratus) infected with Leishmania donovani develop a disease very similar to human Kala-azar. There is conspicuous hipergammaglobulinaemia and their T cells do not respond to stimulation with parasite antigens. We used this experimental model to evaluate the natural killer (NK) activity during the initial phase of the disease. Outbred hamsters infected by intravenous route with 5.106 amastigotes of L. donovani 1S showed a concurrent increase in the spleen weight and in the spleen cell number. Using the single cell assay we detected a significant increase in the percentage of NK effector cells on the 4th day of infection. Imprints from spleen and liver showed at days 14 and 28 a significant increase in the parasite burden . These results show that the increased NK activity in the beginning of the infection was not able to restrain the progression of the disease in this experimental model


Subject(s)
Animals , Female , Killer Cells, Natural/immunology , Leishmania donovani , Leishmaniasis, Visceral/immunology , Lymphocyte Subsets , Cricetinae , Disease Models, Animal , Disease Progression , Liver/microbiology , Liver/pathology , Lymphocyte Count , Spleen/immunology , Spleen/pathology
7.
Rev. Inst. Med. Trop. Säo Paulo ; 40(3): 125-35, May-Jun. 1998. ilus, tab
Article in English | LILACS | ID: lil-224944

ABSTRACT

Fungos patogênicos causadores de micoses sistemicas possuem vários fatores que permitem seu crescimento nas condiçöes adversas oferecidas pelo hospedeiro, propiciando o estabelecimento da relaçäo parasitária e contribuindo no processo de doença. Esses fatores säo conhecidos como fatores de virulencia auxiliando no desenvolvimento da infecçäo e interferindo com a patogenese das micoses. O presente trabalho avalia os fatores de virulencia em fungos patogenicos como Blastomyces dermatitis, Coccidioides immitis, Cryptococcus neoformans, Histoplasma capsulatum e Paracoccidioides brasiliensis, em relaçäo a termotolerancia, dimorfismo, componentes da parede celular ou capsula, bem como a producao de enzimas...


Subject(s)
Humans , Male , Female , Bacterial Infections and Mycoses/virology , Cell Adhesion Molecules/analysis , Blastomycosis/virology , Cell Wall/virology , Coccidioides/isolation & purification , Cryptococcus neoformans/isolation & purification , Enzyme-Linked Immunosorbent Assay , Bacterial Infections and Mycoses/enzymology , Bacterial Infections and Mycoses/parasitology , Biomarkers/analysis , Host-Parasite Interactions
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