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1.
Bull Exp Biol Med ; 171(2): 208-211, 2021 May.
Artículo en Inglés | MEDLINE | ID: mdl-34173094

RESUMEN

In patients with moderate-to-severe and severe psoriasis and high efficacy of therapy (PASI≥75) with signaling pathway inhibitors (apremilast, tofacitinib), cytokine spectra in the skin and blood plasma were studied using xMAP technology at baseline and on weeks 14 and 26 of treatment. Comparison of cytokine levels in psoriatic lesional skin and plasma samples of patients treated with apremilast or tofacitinib revealed statistical difference only for IFNγ level (р<0.05) at week 26.


Asunto(s)
Citocinas/metabolismo , Inhibidores de las Cinasas Janus/farmacología , Inhibidores de Fosfodiesterasa 4/farmacología , Psoriasis/tratamiento farmacológico , Adulto , Estudios de Cohortes , Citocinas/sangre , Citocinas/efectos de los fármacos , Femenino , Humanos , Inhibidores de las Cinasas Janus/uso terapéutico , Masculino , Persona de Mediana Edad , Inhibidores de Fosfodiesterasa 4/uso terapéutico , Piperidinas/farmacología , Piperidinas/uso terapéutico , Psoriasis/sangre , Psoriasis/metabolismo , Psoriasis/patología , Pirimidinas/farmacología , Pirimidinas/uso terapéutico , Índice de Severidad de la Enfermedad , Piel/efectos de los fármacos , Piel/metabolismo , Talidomida/análogos & derivados , Talidomida/farmacología , Talidomida/uso terapéutico , Resultado del Tratamiento , Adulto Joven
2.
Bull Exp Biol Med ; 169(6): 836-839, 2020 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-33098510

RESUMEN

Leprosy was modeled in an experiment on BALB/c, BALB/cNude, CBA, and C57BL/6ТNF-/- mice using three Mycobacterium leprae strains obtained from patients with a diagnosis of A30 according to ICD-10 from different regions of the Russian Federation. Proliferation of M. leprae of the used strains showed a temporal-quantitative dependence on the used mouse line. CBA and BALB/cNude mice were optimal for strain R and BALB/c and BALB/cNude lines were optimal for strain I. BALB/cNude mice infected with strain I had low lifespan. M. leprae strain M showed low proliferation activity in BALB/cNude and C57BL/6ТNF-/- mice.


Asunto(s)
Inmunidad Adaptativa , Inmunidad Innata , Lepra/inmunología , Longevidad/inmunología , Mycobacterium leprae/patogenicidad , Factor de Necrosis Tumoral alfa/inmunología , Animales , ADN Bacteriano/genética , Modelos Animales de Enfermedad , Especificidad del Huésped , Humanos , Lepra/genética , Lepra/microbiología , Lepra/patología , Longevidad/genética , Ratones , Ratones Endogámicos BALB C , Ratones Endogámicos C57BL , Ratones Endogámicos CBA , Ratones Noqueados , Ratones Desnudos , Mycobacterium leprae/genética , Mycobacterium leprae/crecimiento & desarrollo , Mycobacterium leprae/inmunología , Factor de Necrosis Tumoral alfa/deficiencia , Factor de Necrosis Tumoral alfa/genética
3.
Klin Lab Diagn ; 63(8): 511-516, 2018.
Artículo en Ruso | MEDLINE | ID: mdl-30726657

RESUMEN

Certain level of new registered cases of leprosy in a number of endemic countries in the world, as well as growing rate of transboundary migratory flows, raise the issue of effective diagnosis of this disease in countries with sporadic incidence of leprosy, including the Russian Federation. The purpose of the study was to develop a highly sensitive PCR test for detecting the genetic material of Mycobacterium leprae and to compare the test robustness and sensitivity with the commercially available Leprosy Genesig Standard Kit (Primerdesign Ltd., UK). The proposed approach uses real time PCR of non-coding repeating element RLEP, unique for the M. leprae genome, using TaqMan probe. The high test specificity was shown using the reference DNA samples of pathogenic and conditionally pathogenic mycobacterium, as well and its comparison with single-copy genes of M. leprae (rrs, fbp, MntH) PCR detection. The use of a commercially available test system based on the single-copy rpoB gene detection provided 59.4% sensitivity to the detection of M. leprae in the clinical material, while the application of the developed approach increased this index to 96.8%. The developed PCR diagnostics test of leprosy is submitted for state clinical approval process, whereupon the practical use of the test diagnostics allows solving a wide range of tasks to identify and confirm new cases of leprosy, and monitoring both the effectiveness of leprosy treatment, and epidemiological (including transboundary) the spread of the disease.


Asunto(s)
Lepra/diagnóstico , Mycobacterium leprae/genética , Reacción en Cadena en Tiempo Real de la Polimerasa , Proteínas Bacterianas/genética , ADN Bacteriano/genética , ARN Polimerasas Dirigidas por ADN/genética , Humanos , Mycobacterium leprae/aislamiento & purificación , Federación de Rusia , Sensibilidad y Especificidad
4.
Mol Gen Mikrobiol Virusol ; (2): 3-11, 2008.
Artículo en Ruso | MEDLINE | ID: mdl-18494110

RESUMEN

Minisatellite loci are a part of the human genome, playing an important role in various genomic and population studies. The review describes characteristics of this group of hypervariable tandem repeats and models that explain the reasons for their high diversity. The use of this kind of markers in population genetics studies is demonstrated by an example of the D1S80 minisatellite locus. Particular emphasis was placed on the D1S80 diversity in different populations of Eastern Europe. The capabilities of D1S80 for population analyses that allow the resolution of both main human groups and small differences to be resolved in population structures.


Asunto(s)
Genética de Población , Genoma Humano/genética , Repeticiones de Microsatélite , Europa Oriental , Marcadores Genéticos , Variación Genética , Humanos
5.
Ann Hum Biol ; 33(5-6): 570-84, 2006.
Artículo en Inglés | MEDLINE | ID: mdl-17381055

RESUMEN

BACKGROUND: It has been hypothesized that, whereas many loci are used to generate phylogenetic relationships, the utilization of those that yield the most information could increase the accuracy of any multilocus phylogenetic reconstruction. Among these is the D1S80 hypervariable minisatellite region, which has been shown to be highly polymorphic globally, and it was of interest to compare the nearest neighbours and distant populations of Eastern Europe using the D1S80 polymorphism. AIM: The study evaluated the capacity of the D1S80 locus to discriminate between populations from different ethnic groups in Russia and the Republic of Belarus, revealing the polymorphism parameters of the populations studied. SUBJECTS AND METHODS: Hypervariable D1S80 minisatellite polymorphism was studied in 15 populations, belonging to six distinct ethnic groups from the Russian Federation (Russians, Komis, Maris, Udmurts, Kalmyks, and Yakuts) and the Republic of Belarus (Byelorussians). The data were analysed with other results reported for D1S80 polymorphism among Eastern Europeans, and were analysed together with those previously reported for Eastern European populations for the 3'ApoB, DMPK, DRPLA, and SCA1 hypervariable loci. Genetic diversity analysis was carried out using multidimensional scaling (MDS) of Nei's genetic distances. RESULTS: The Eastern Slavonic populations (Russians, Ukrainians, and Byelorussians) are closely associated, and outermost from populations of Asian origin (Kalmyks and Yakuts). The populations that inhabit the Volga-Ural region (Udmurt, Komi, Mari, and Bashkir ethnic groups) revealed intermediate characteristics. CONCLUSION: The clustering of populations demonstrated here using D1S80 alone coincides with the analysis of five hypervariable region (HVR) loci, and is consistent with linguistic, geographic, and ethnohistorical data. These results are in agreement with most studies of mtDNA, Y-chromosomal, and autosomal DNA diversity in Eastern Europe. The D1S80 locus is convenient for population analyses, and may be used as part of a set of similar markers, which should allow the easy resolution of small differences in population structures.


Asunto(s)
Pueblo Asiatico/genética , Etnicidad/genética , Polimorfismo Genético , Población Blanca/genética , Europa Oriental , Frecuencia de los Genes , Humanos , Repeticiones de Minisatélite , Reacción en Cadena de la Polimerasa
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