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首页> 外文期刊>Biological research for nursing >Lymphocyte Recovery After Breast Cancer Treatment and Mindfulness-Based Stress Reduction (MBSR) Therapy
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Lymphocyte Recovery After Breast Cancer Treatment and Mindfulness-Based Stress Reduction (MBSR) Therapy

机译:乳腺癌治疗和基于正念减压(MBSR)治疗后的淋巴细胞恢复

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Objectives:This randomized controlled trial was conducted to examine immune recovery following breast cancer (BC) therapy and evaluate the effect of mindfulness-based stress reduction therapy (MBSR) on immune recovery with emphasis on lymphocyte subsets, T cell activation, and production of T-helper 1 (Th1; interferon [IFN]-γ) and T-helper 2 (Th2; interleukin-4 [IL-4]) cytokines.Method:Participants who completed the study consisted of 82 patients diagnosed with Stage 0-III BC, who received lumpectomy and adjuvant radiation ± chemotherapy. Patients were randomized into an MBSR(BC) intervention program or a control (usual care) group. Immune cell measures were assessed at baseline and within 2 weeks after the 6-week intervention. The numbers and percentages of lymphocyte subsets, activated T cells, and Th1 and Th2 cells in peripheral blood samples were determined by immunostaining and flow cytometry.Results:Immune subset recovery after cancer treatment showed positive associations with time since treatment completion. The B and natural killer (NK) cells were more susceptible than T cells in being suppressed by cancer treatment. Women who received MBSR(BC) had T cells more readily activated by the mitogen phytohemagglutinin (PHA) and an increase in the Th1/Th2 ratio. Activation was also higher for the MBSR(BC) group if <12 weeks from the end of treatment and women in MBSR(BC) <12 weeks had higher T cell count for CD4+.Conclusion:MBSR(BC) promotes a more rapid recovery of functional T cells capable of being activated by a mitogen with the Th1 phenotype, whereas substantial recovery of B and NK cells after completion of cancer treatment appears to occur independent of stress-reducing interventions.
机译:目的:进行这项随机对照试验,以检查乳腺癌(BC)治疗后的免疫恢复,并评估正念减压治疗(MBSR)对免疫恢复的影响,重点是淋巴细胞亚群,T细胞活化和T产生-辅助细胞1(Th1;干扰素[IFN]-γ)和T-辅助细胞2(Th2; interleukin-4 [IL-4])细胞因子。方法:完成研究的参与者由82位被诊断为BC期0-III的患者组成,谁接受了肿块切除术和辅助放射±化疗。将患者随机分为MBSR(BC)干预计划或对照组(常规护理)组。在基线和6周干预后的2周内评估了免疫细胞测量。通过免疫染色和流式细胞仪测定外周血样本中淋巴细胞亚群,活化的T细胞以及Th1和Th2细胞的数量和百分比。 B和自然杀伤(NK)细胞比T细胞更易受到癌症治疗的抑制。接受MBSR(BC)的女性的T细胞更容易被有丝分裂原植物血凝素(PHA)激活,并且Th1 / Th2比率增加。如果治疗结束后<12周,MBSR(BC)组的激活也更高,而MBSR(BC)中<12周的女性的CD4 + T细胞计数更高。结论:MBSR(BC)促进了CDSR的更快恢复。能够被具有Th1表型的有丝分裂原激活的功能性T细胞,而完成癌症治疗后B和NK细胞的大量恢复似乎与减轻压力的干预措施无关。

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