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The Relationship between the Lifestyle of the Allogeneic Stem Cell Donors and the Number of Donated CD34+ and CD3+ Cells 异体干细胞捐献者的生活方式与捐献的 CD34+ 和 CD3+ 细胞数量之间的关系
Pub Date : 2024-07-21 DOI: 10.18502/ijhoscr.v18i3.16101
Leila Sayadi, Saeed Mohammadi, Parivash Aminian
Background: Hematopoietic stem cell transplantation (HSCT) is considered as the last treatment option in many life-threatening diseases. The number of donated cells can affect transplantation success. This study attempted to investigate the relationship between the health-promoting lifestyle of allogeneic stem cell donors and the number of donated CD34+ and CD3+ cells. Materials and Methods: The study was a descriptive correlational study in which 100 peripheral blood stem cells donors participated. A demographic form and health-promoting lifestyle profile-II questionnaire were distributed to participants, and then cell separation was started. Afterward, the results of CD34 + and CD3 + cell counts, as well as other clinical parameters of the participants, were recorded. The collected data were analyzed by descriptive and analytical statistical methods. Results:  The results showed that the mean total health-promoting lifestyle profile score for hematopoietic stem cell donors was 2.876±0.461. There was no significant relationship between the health- promoting lifestyle score and the number of CD34+, CD3+ cells and CD3+/CD34+ ratio. A positive and significant correlation was found between the weight of the donors and the number of CD34+ (P < 0.001) and CD3+ cells (P = 0.001). The number of CD34+ cells was significantly different between women and men (P = 0.009). Conclusion: Lifestyle had no significant effect on the number of CD3+/CD34+ cells. Moreover, the number of CD34+ cells was significantly higher in men, so males should be preferentially recruited as donors for the HSCT procedure.
背景:造血干细胞移植(HSCT)被认为是许多危及生命的疾病的最后治疗方案。捐献细胞的数量会影响移植的成功率。本研究试图调查异体干细胞捐献者促进健康的生活方式与捐献的 CD34+ 和 CD3+ 细胞数量之间的关系。材料与方法:本研究是一项描述性相关研究,共有 100 名外周血干细胞捐献者参加。研究人员向参与者发放了人口统计学表格和健康促进生活方式档案-II问卷,然后开始进行细胞分离。之后,记录参与者的 CD34 + 和 CD3 + 细胞计数结果以及其他临床参数。收集的数据采用描述性和分析性统计方法进行分析。结果显示 结果显示,造血干细胞捐献者健康促进生活方式档案总分的平均值为(2.876±0.461)分。促进健康生活方式评分与 CD34+、CD3+ 细胞数量和 CD3+/CD34+ 比率之间无明显关系。供体体重与 CD34+ 细胞数(P < 0.001)和 CD3+ 细胞数(P = 0.001)之间存在明显的正相关。女性和男性的 CD34+ 细胞数量存在显著差异(P = 0.009)。结论生活方式对 CD3+/CD34+ 细胞数量无明显影响。此外,男性的 CD34+ 细胞数量明显高于女性,因此造血干细胞移植手术应优先选择男性捐献者。
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引用次数: 0
Clinical and Paraclinical Features, Outcome, and Prognosis of Extranodal Natural Killer/T-Cell Lymphoma, Nasal Type: A Retrospective Study of 31 Vietnamese Patients 鼻型结节外天然杀伤/T细胞淋巴瘤的临床和辅助临床特征、结果和预后:对 31 名越南患者的回顾性研究
Pub Date : 2024-07-21 DOI: 10.18502/ijhoscr.v18i3.16107
Kien Hung Do, Tu Anh Do, Tai Van Nguyen, Duc Thanh Le, Linh Van Phan, C. Nguyen
Background: Extranodal natural killer (NK)/T-cell lymphoma, nasal type is a rare, aggressive, and poor prognostic subtype. The concurrent chemoradiotherapy followed by chemotherapy showed a relatively high response rate and the toxicity due to the treatment is acceptable. The study attempted to report the clinicopathological features, the survival outcome, and response rates of stages I-II, nasal type ENKTL patients treated with CCRT followed by adjuvant VIPD chemotherapy in Vietnam. Materials and Methods: The current study was conducted on 31 stage I or II NK/T cell lymphoma, nasal-type patients received by CCRT, followed by adjuvant VIPD chemotherapy. Information on patient demographics, disease stage, clinical symptoms, tumor, and paraclinical characteristics were collected. The primary endpoints of this study were OS and response rates. Results: After CCRT, 26 out of 31 (83.9%) patients had stable disease or response. Overall response rate (ORR) was observed in 80.6% of patients with a complete response rate of 67.7%. Low-risk PINK patients had a higher response rate than the intermediate- risk group (p=0.038). Mean disease-free survival was 44.3±4.5 months (95% CI, 35.4-53.1 months). Mean overall survival was 46.8±4.5 months (95% CI, 37.99-55.8 months). The intermediate-risk PINK patients had a significantly lower OS rate than low-risk patients. Conclusion: Concurrent chemoradiotherapy followed by adjuvant VIPD chemotherapy showed a high response rate and survival benefit in stages I-II, nasal type, and extranodal natural killer (NK)/T-cell lymphoma Vietnamese patients.
背景:鼻型结节外天然杀伤(NK)/T细胞淋巴瘤是一种罕见、侵袭性强、预后不良的亚型淋巴瘤。同时进行的化放疗和化疗显示了相对较高的反应率,而且治疗引起的毒性是可以接受的。本研究试图报告越南鼻腔型ENKTL I-II期患者接受CCRT治疗后辅助VIPD化疗的临床病理特征、生存结果和反应率。材料与方法:本研究对31例I期或II期鼻型NK/T细胞淋巴瘤患者进行了CCRT治疗和VIPD辅助化疗。研究收集了患者的人口统计学信息、疾病分期、临床症状、肿瘤和辅助临床特征。本研究的主要终点是OS和反应率。研究结果接受 CCRT 治疗后,31 例患者中有 26 例(83.9%)病情稳定或有反应。总体反应率(ORR)为 80.6%,完全反应率为 67.7%。低风险 PINK 患者的应答率高于中度风险组(P=0.038)。平均无病生存期为 44.3±4.5 个月(95% CI,35.4-53.1 个月)。平均总生存期为46.8±4.5个月(95% CI,37.99-55.8个月)。中危 PINK 患者的 OS 率明显低于低危患者。结论在I-II期、鼻型和结节外自然杀伤(NK)/T细胞淋巴瘤越南患者中,同期化放疗和VIPD辅助化疗显示出较高的反应率和生存率。
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引用次数: 0
Silibinin, Synergistically Enhances Vinblastine-Mediated Apoptosis in Triple Negative Breast Cancer Cell Line: Involvement of Bcl2/Bax and Caspase-3 Pathway Silibinin, Synergistically Enhances Vinblastine-Mediated Apoptosis in Triple Negative Breaster Cancer Cell Line:Bcl2/Bax 和 Caspase-3 通路的参与
Pub Date : 2024-04-24 DOI: 10.18502/ijhoscr.v18i2.15375
H. Dariushnejad, Neda Roshanravan, Hunar Mustafa Wasman, Mostafa Cheraghi, Lale Pirzeh, V. Ghorbanzadeh
Background: Triple-negative breast cancer (TNBC) with a poor prognosis and survival is the most invasive subtype of breast cancer.  Usually, TNBC requires a chemotherapy regimen at all stages, but chemotherapy drugs have shown many side effects. We assumed that combination therapy of vinblastine and silibinin might reduce the vinblastine toxicity and dose of vinblastine. Materials and Methods: The MDA-MB-231 were cells subjected to MTT assay for IC50 determination and combination effects, which were measured based on Chou-Talalay's method. The type of cell death was determined by using a Flow-cytometric assay. Cell death pathway markers, including Bcl-2, Bax, and caspase-3 were analyzed by western blot and Real-Time PCR. Results: The treatment of MDA-MB-231 cells exhibited IC50 and synergism at the combination of 30 µM of silibinin and 4 µm of vinblastine in cell viability assay (CI=0.69). YO-PRO-1/PI double staining results showed a significant induction of apoptosis when MDA-MB-231 cells were treated with a silibinin and vinblastine combination (p<0.01). Protein levels of Bax and cleaved caspase-3 were significantly upregulated, and Bcl-2 downregulated significantly. Significant upregulation of Bax (2.96-fold) and caspase-3 (3.46-fold) while Bcl-2 was downregulated by 2-fold. Conclusion: Findings established a preclinical rationale for the combination of silibinin and vinblastine. This combination produces synergistic effects in MDA-MB-231 cells by altering pro- and anti-apoptotic genes, which may reduce the toxicity and side effects of vinblastine.
背景:三阴性乳腺癌(TNBC)预后差、生存率低,是乳腺癌中侵袭性最强的亚型。 通常,TNBC 在各个阶段都需要化疗,但化疗药物有很多副作用。我们认为,长春新碱和西利宾联合治疗可能会降低长春新碱的毒性,减少长春新碱的剂量。材料与方法用 MTT 法测定 MDA-MB-231 细胞的 IC50 值,并根据 Chou-Talalay 法测定联合疗法的效果。细胞死亡类型通过流式细胞仪测定。细胞死亡通路标记物,包括 Bcl-2、Bax 和 caspase-3 通过 Western 印迹和 Real-Time PCR 进行分析。结果在细胞活力测定中,30 µM 的西利宾和 4 µm 的长春新碱组合处理 MDA-MB-231 细胞的 IC50 和协同作用(CI=0.69)。YO-PRO-1/PI双重染色结果表明,当MDA-MB-231细胞接受西利宾和长春新碱的联合治疗时,可显著诱导细胞凋亡(p<0.01)。Bax 和裂解的 caspase-3 蛋白水平明显上调,Bcl-2 蛋白水平明显下调。Bax (2.96 倍)和 caspase-3 (3.46 倍)明显上调,而 Bcl-2 则下调了 2 倍。结论研究结果为西利宾和长春新碱的联合应用提供了临床前依据。这种联合疗法通过改变促凋亡基因和抗凋亡基因在 MDA-MB-231 细胞中产生协同效应,可降低长春新碱的毒性和副作用。
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引用次数: 0
A Case of Deep Venous Thrombosis in an HIV-Infected Patient despite Therapeutic Anticoagulation 一例艾滋病毒感染者在接受抗凝治疗后仍出现深静脉血栓的病例
Pub Date : 2024-04-24 DOI: 10.18502/ijhoscr.v18i2.15379
Wajeeha Aiman, Muhammad Ashar Ali, Navjot Grewal, Andreas A. Savopoulos, G. Guron
Patients with human immunodeficiency virus (HIV) infection have an increased likelihood of venous thromboembolism (VTE) owing to factors such as acquired protein C and S deficiency, antiphospholipid antibody syndrome, and heightened levels of pro-inflammatory cytokines. This case report highlights an exceptionally uncommon occurrence of deep venous thrombosis in an HIV-infected patient receiving a therapeutic dose of enoxaparin. This underscores the need for cautious consideration of the risk of VTE in HIV-infected individuals, even with preventive or therapeutic anticoagulant treatment. Further research is recommended to investigate HIV as a potential risk factor of prophylactic anticoagulation.
由于获得性蛋白 C 和 S 缺乏、抗磷脂抗体综合征以及促炎细胞因子水平升高等因素,人类免疫缺陷病毒(HIV)感染患者发生静脉血栓栓塞(VTE)的可能性增加。本病例报告强调了一名接受治疗剂量依诺肝素的 HIV 感染者发生深静脉血栓的异常罕见情况。这强调了即使接受了预防性或治疗性抗凝剂治疗,也需要谨慎考虑 HIV 感染者发生 VTE 的风险。建议开展进一步研究,将 HIV 作为预防性抗凝治疗的潜在风险因素进行调查。
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引用次数: 0
HHV-8 Linked to Kaposi's Sarcoma and Castleman's Disease in HIV-1-infected patient: Case Report and Review of the Literature HHV-8 与 HIV-1 感染者的卡波西肉瘤和 Castleman 病有关:病例报告与文献综述
Pub Date : 2024-04-24 DOI: 10.18502/ijhoscr.v18i2.15378
A. Zaghdoudi, Hajer Harrabi, Hanene Tiouiri Benaissa
Kaposi’s sarcoma (KS) and multicentric Castleman's disease (MCD) are both linked to human herpesvirus-8 (HHV-8) infection which most commonly affects people living with human immunodeficiency virus (HIV).  Herein, we describe the case of a 57-year-old patient who has been admitted for fever, night sweats, weight loss, and diffuse lymphadenopathy with abdominal pain. HIV status was confirmed by a positive Western blot test. His initial CD4 cell count was equal to 270 cells/µL. A histological study of a peripheral lymph node concluded that KS is associated with MCD. These two conditions found in the same patient highlight the malignant potential of HHV-8, particularly in the case of HIV-induced immunodeficiency.  
卡波西肉瘤(KS)和多中心卡斯特曼病(MCD)都与人类疱疹病毒-8(HHV-8)感染有关,而人类疱疹病毒-8感染最常见于人类免疫缺陷病毒(HIV)感染者。 在此,我们描述了一例因发热、盗汗、体重减轻、弥漫性淋巴结病伴有腹痛而入院的 57 岁患者。经 Western 印迹检测呈阳性,确诊为艾滋病病毒感染者。他最初的 CD4 细胞计数为 270 cells/µL。外周淋巴结的组织学检查结果表明,KS与MCD有关。在同一名患者身上发现的这两种病症凸显了 HHV-8 的恶性潜能,尤其是在艾滋病毒诱发免疫缺陷的情况下。
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引用次数: 0
Hemoglobin C Disorder in Anemic Patients Referred to the National Center for Thalassemia and Genetic Counseling in Damascus 大马士革国家地中海贫血症和遗传咨询中心转诊的贫血患者中的血红蛋白 C 紊乱症
Pub Date : 2024-04-24 DOI: 10.18502/ijhoscr.v18i2.15376
Aya Ahmad, Karam Fattoum, Wael Imam, Mhd Yasser Mukhalalaty, Musab Murad, Faizah Ali Al Quobaili
Background: Hemoglobinopathies are common inherited blood disorders in our Mediterranean area. The main structural hemoglobin variants are hemoglobin S and hemoglobin C, due to their prevalence. We conducted this retrospective study to investigate and characterize hemoglobin C patients referred to the National Center for Thalassemia and Genetic Counseling and the management of hemoglobin C disease in Damascus. Materials and Methods: The study included patients referred to the National Center for Thalassemia and Genetic Counseling in Damascus between 2000 and 2022 for hemoglobin C detection. Gender, age, geographical origin, hemoglobin electrophoresis profile, and blood transfusion were considered for hemoglobin C patient classification. Blood transfusion in five consecutive years and linear regression with hemoglobin S and C values were determined. Results: 30 (14 males and 16 females) out of 624 patients between 3 and 46 years old (mean ± SD: 17.3 ± 9.7 years) showed hemoglobin C disease. Only eight patients (one male and seven females) received blood transfusions, and the remaining patients (13 males and 9 females) did not receive any transfusion. Only one patient with 100% hemoglobin C was detected; 19 showed HbSC, and 10 had HbAC. There was a significant correlation between hemoglobin S and geographical origin (P-value=0). Conclusion: A Homozygote hemoglobin C patient has mild hemolytic anemia, whereas the hemoglobin C 100% patient has only a one-time blood transfusion (he was 17 years old) in our study. The inherited combination of hemoglobin C and S is less severe than hemoglobin S alone. There is a significant relationship between hemoglobin S and geographical origin (p-value=0).
背景:血红蛋白病是地中海地区常见的遗传性血液疾病。由于血红蛋白 S 和血红蛋白 C 的发病率较高,因此主要的结构性血红蛋白变异体是血红蛋白 S 和血红蛋白 C。我们进行了这项回顾性研究,以调查和描述转诊至国家地中海贫血和遗传咨询中心的血红蛋白 C 患者以及大马士革血红蛋白 C 疾病的管理情况。材料和方法:研究对象包括 2000 年至 2022 年期间因检测出 C 型血红蛋白而转诊至大马士革国家地中海贫血和遗传咨询中心的患者。在对 C 型血红蛋白患者进行分类时,考虑了性别、年龄、地域、血红蛋白电泳图谱和输血情况。确定了连续五年的输血量以及与血红蛋白 S 和 C 值的线性回归。结果在 624 名 3 至 46 岁的患者中,有 30 人(男性 14 人,女性 16 人)患有血红蛋白 C 疾病(平均 ± SD:17.3 ± 9.7 岁)。只有 8 名患者(1 名男性和 7 名女性)接受了输血,其余患者(13 名男性和 9 名女性)未接受任何输血。只有一名患者的血红蛋白 C 含量为 100%;19 名患者的血红蛋白 C 含量为 HbSC,10 名患者的血红蛋白 C 含量为 HbAC。血红蛋白 S 与地理来源有明显的相关性(P 值=0)。结论在我们的研究中,同型血红蛋白 C 患者有轻度溶血性贫血,而血红蛋白 C 100%患者仅输血一次(17 岁)。血红蛋白 C 和血红蛋白 S 的遗传组合比单独的血红蛋白 S 严重程度要轻。血红蛋白 S 与地理来源之间有明显的关系(P 值=0)。
{"title":"Hemoglobin C Disorder in Anemic Patients Referred to the National Center for Thalassemia and Genetic Counseling in Damascus","authors":"Aya Ahmad, Karam Fattoum, Wael Imam, Mhd Yasser Mukhalalaty, Musab Murad, Faizah Ali Al Quobaili","doi":"10.18502/ijhoscr.v18i2.15376","DOIUrl":"https://doi.org/10.18502/ijhoscr.v18i2.15376","url":null,"abstract":"Background: Hemoglobinopathies are common inherited blood disorders in our Mediterranean area. The main structural hemoglobin variants are hemoglobin S and hemoglobin C, due to their prevalence. \u0000We conducted this retrospective study to investigate and characterize hemoglobin C patients referred to the National Center for Thalassemia and Genetic Counseling and the management of hemoglobin C disease in Damascus. \u0000Materials and Methods: The study included patients referred to the National Center for Thalassemia and Genetic Counseling in Damascus between 2000 and 2022 for hemoglobin C detection. Gender, age, geographical origin, hemoglobin electrophoresis profile, and blood transfusion were considered for hemoglobin C patient classification. Blood transfusion in five consecutive years and linear regression with hemoglobin S and C values were determined. \u0000Results: 30 (14 males and 16 females) out of 624 patients between 3 and 46 years old (mean ± SD: 17.3 ± 9.7 years) showed hemoglobin C disease. Only eight patients (one male and seven females) received blood transfusions, and the remaining patients (13 males and 9 females) did not receive any transfusion. Only one patient with 100% hemoglobin C was detected; 19 showed HbSC, and 10 had HbAC. There was a significant correlation between hemoglobin S and geographical origin (P-value=0). \u0000Conclusion: A Homozygote hemoglobin C patient has mild hemolytic anemia, whereas the hemoglobin C 100% patient has only a one-time blood transfusion (he was 17 years old) in our study. The inherited combination of hemoglobin C and S is less severe than hemoglobin S alone. There is a significant relationship between hemoglobin S and geographical origin (p-value=0).","PeriodicalId":94048,"journal":{"name":"International journal of hematology-oncology and stem cell research","volume":"23 19","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140663519","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Risk of Sarcopenia Identified by Sarc-Calf, Nutritional Status and Hand Grip Strength in Patients with Hematological Cancer 通过血液肿瘤患者的 Sarc-Calf、营养状况和手部握力识别肌少症风险
Pub Date : 2024-04-21 DOI: 10.18502/ijhoscr.v18i2.15370
Lorraine Pires Avancini, Laís Freitas da Costa, Mariana de Souza Vieira, Vanusa Felício de Souza, Rayne de Almeida Marques, Jose Luiz Marques Rocha, G. Petarli, V. Guandalini
Background: Hematological cancer patients are prone to the development of sarcopenia and impaired nutritional and functional status. SARC-CalF is a screening tool for the risk of sarcopenia that has shown good results in this population. This study aimed to identify the risk of sarcopenia by SARC-CalF and to verify its association with nutritional status and Hand Grip Strength (HGS) in patients with hematological cancer. Materials and Methods: Adult patients, of both sexes, with hematological cancer, and in outpatient care participated in the study. We measured the Hand Grip Strength of the Dominant Hand (HGSD) and the Adductor Pollicis Muscle Thickness of the Dominant Hand (APMTD). Moreover, we applied the Patient-Generated Subjective Global Assessment (PG-SGA) and SARC-CalF. Data were analyzed with SPSS® software, 22.0, with a significance level of 5.0%. Results: Fifty-one patients aged an average of 60.4 ± 15.1 years were evaluated. Of those, 58.8% were elderly, 51% female, and 80.4% declared themselves non-white. The predominant diagnosis was Mature B Lymphoid Cell Neoplasia (37.7%), and 60.8% of the patients had a diagnosis time of ≤ 3 years. PG-SGA revealed that 35.3% of the patients were malnourished; APMTD and HGSD revealed that 60.8% and 25.5% had reduced muscle strength, respectively. SARC-CalF exposed that 39.2% of the patients were at risk for sarcopenia. Significant associations were found between SARC-CalF and diagnosis time ≤ 3 years (p = 0.039), PG-SGA (p = 0.020), APMTD (p = 0.039) and HGSD (p = 0.002). After binary logistic regression adjusted for age and sex, the reduced HGSD remained associated with the risk of sarcopenia. Conclusion: SARC-CalF identified a risk of sarcopenia in 39.2% of patients. The reduced HGSD was associated with the risk of sarcopenia.
背景:血液肿瘤患者容易出现肌肉疏松症,营养和功能状况也会受损。SARC-CalF 是一种筛查肌肉疏松症风险的工具,在这一人群中显示出良好的效果。本研究旨在通过 SARC-CalF 确定血液肿瘤患者的肌肉疏松症风险,并验证其与营养状况和手握力(HGS)之间的关联。材料与方法:参与研究的患者均为门诊患者,男女不限。我们测量了支配手的握力(HGSD)和支配手的内收肌厚度(APMTD)。此外,我们还采用了患者自发主观全面评估(PG-SGA)和 SARC-CalF。数据采用 SPSS® 软件 22.0 进行分析,显著性水平为 5.0%。结果接受评估的 51 名患者平均年龄为(60.4 ± 15.1)岁。其中 58.8%为老年人,51%为女性,80.4%自称非白人。主要诊断为成熟 B 淋巴细胞瘤(37.7%),60.8%的患者确诊时间不超过 3 年。PG-SGA显示35.3%的患者营养不良;APMTD和HGSD分别显示60.8%和25.5%的患者肌力下降。SARC-CalF 显示 39.2% 的患者有肌少症风险。研究发现,SARC-CalF 与诊断时间≤ 3 年(p = 0.039)、PG-SGA(p = 0.020)、APMTD(p = 0.039)和 HGSD(p = 0.002)之间存在显著关联。在对年龄和性别进行二元逻辑回归调整后,HGSD 的降低仍与肌肉疏松症的风险相关。结论SARC-CalF 确定了 39.2% 的患者存在肌少症风险。HGSD的降低与肌少症的风险有关。
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引用次数: 0
Serum Interleukin 6 (IL -6) as Prognostic Marker in Egyptian CLL patients 血清白细胞介素 6 (IL -6) 作为埃及 CLL 患者的预后指标
Pub Date : 2024-04-21 DOI: 10.18502/ijhoscr.v18i2.15369
E. A. Hassan, E. Abdelhady, H. Abdelsamee, Mohamed Tarif Hamza sallam, M. El-Razzaz
Background: Chronic lymphocytic leukemia (CLL) is the most common leukemia in adults. Currently, several biomarkers are being used as CLL prognosticators, including elevated protein levels, elevated RNA levels, gene mutations, and epigenetic changes. Materials and Methods: This study is a prospective study conducted on 55 patients newly diagnosed with CLL, serum IL-6 level was measured initially and after a 6-month treatment course. Correlation with the course of the disease and the known CLL prognostic parameters was done initially and after 6 months. Results: The initial serum IL-6 level in the patient group (pre-treatment) ranges from 36-91 pg/mL (median 57), and in the patient group (post-treatment) ranges from 1-32 pg/mL (median 2). Serum IL-6 level was positively correlated with WBC count, β2 microglobulin, LDH, ESR, B symptoms, Uric Acid, BM Aspirate (% of lymphocytes), and Binet and Rai staging systems. Conclusion: Serum IL-6 is a useful poor prognostic marker in newly diagnosed CLL patients; its prognostic value goes with the other known prognostic markers such as the BM lymphocyte count, ESR, and LDH.
背景:慢性淋巴细胞白血病(CLL慢性淋巴细胞白血病(CLL)是成人中最常见的白血病。目前,有几种生物标志物被用作 CLL 的预后指标,包括蛋白质水平升高、RNA 水平升高、基因突变和表观遗传学变化。材料和方法:本研究是一项前瞻性研究,对 55 例新诊断为 CLL 的患者进行了血清 IL-6 水平测定,测定的对象包括最初和 6 个月疗程后的患者。最初和 6 个月后的血清 IL-6 水平与病程和已知的 CLL 预后参数之间存在相关性。结果显示患者组(治疗前)的初始血清IL-6水平为36-91皮克/毫升(中位数为57),患者组(治疗后)的初始血清IL-6水平为1-32皮克/毫升(中位数为2)。血清 IL-6 水平与白细胞计数、β2 微球蛋白、LDH、血沉、B 症状、尿酸、骨髓穿刺液(淋巴细胞百分比)以及 Binet 和 Rai 分期系统呈正相关。结论血清IL-6是新诊断的CLL患者预后不良的有用标记物;其预后价值与其他已知的预后标记物(如BM淋巴细胞计数、血沉和LDH)相同。
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引用次数: 0
Influence of Different Glucose Concentrations on the Expression of miR-29c-3p microRNA in Mesenchymal Stem Cells 不同葡萄糖浓度对间质干细胞中 miR-29c-3p microRNA 表达的影响
Pub Date : 2024-04-21 DOI: 10.18502/ijhoscr.v18i2.15367
Somayeh Mansournejad, M. Mehrabi, Reza Yari, Mahshid Saleh
Background: miR-29c-3p manages a set of genes involved in regenerative medicine, and It seems that hyperglycemia in diabetic patients influences the power of stem cells to tissue regeneration the difficulties of diabetes by affecting the expression miR-29c-3p in mesenchymal stem cells. The study aims to analyze the effect of various glucose concentrations on the miR-29c-3p expression in mesenchymal stem cells. Materials and Methods: After receiving donated mesenchymal stem cells from Tarbiat Modares University, these cells were cultivated in a DMEM culture medium, including three different concentrations of glucose 250, 140, and 100 mg/dl. RNA was extracted from these cells after 72 hours, the Real-Time PCR technique assessed the expression of miR-29c-3p, and the results were analyzed by REST software. Results: miR-29c-3p expression in cells at concentrations of 140 and 250 mg/dL compared to typical situations (100 mg/dl) was significantly decreased (P˂0.05), which declined at a concentration of 250 mg/dl was more. Conclusion: Reduced miR-29c-3p expression in mesenchymal stem cells in chronic and mild diabetic situations demonstrated that diabetes might be one of the significant reasons for mesenchymal stem cells' reduced ability to repair tissue damage.
背景:miR-29c-3p管理着一组参与再生医学的基因,而糖尿病患者的高血糖似乎通过影响间充质干细胞中miR-29c-3p的表达来影响干细胞组织再生的能力,从而解决糖尿病带来的困难。本研究旨在分析不同浓度的葡萄糖对间充质干细胞中 miR-29c-3p 表达的影响。材料与方法:接受塔尔比亚特莫达尔斯大学捐赠的间充质干细胞后,这些细胞在DMEM培养基中培养,其中包括三种不同浓度的葡萄糖250、140和100 mg/dl。72 小时后从这些细胞中提取 RNA,用 Real-Time PCR 技术评估 miR-29c-3p 的表达,并用 REST 软件分析结果。结果:与典型情况(100 mg/dl)相比,浓度为 140 mg/dL 和 250 mg/dL 的细胞中 miR-29c-3p 的表达明显下降(P˂0.05),浓度为 250 mg/dl 时下降幅度更大。结论慢性和轻度糖尿病患者间充质干细胞中的miR-29c-3p表达减少,表明糖尿病可能是间充质干细胞修复组织损伤能力下降的重要原因之一。
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引用次数: 0
Assessment of Torque Teno Virus (TTV) Frequency in Healthy Blood Donors in the Central Region of Iran, Yazd 伊朗中部亚兹德地区健康献血者体内托克特诺病毒 (TTV) 感染频率评估
Pub Date : 2024-04-21 DOI: 10.18502/ijhoscr.v18i2.15366
Zahra Naderipour, Farzane Behnezhad, J. Charostad, M. Nakhaie, Nadieh Baniasadi, Y. Ghelmani, Fateme Akhavan Tafti, Azam Dehghani, Akram Astani
Background: Torque teno virus (TTV) is a globally prevalent virus in humans, yet comprehensive knowledge about its prevalence, predominant transmission routes, and pathogenesis remains limited. This study aimed to assess the frequency of TTV infection among healthy blood donors in Yazd, Iran. Materials and Methods: A total of 236 healthy blood donors, devoid of HIV/HBV/HCV infection markers, participated in the study from 2015 to 2016. Nested Polymerase Chain Reaction (PCR) utilizing a set of oligo primers for the 5΄- UTR region was employed to detect TTV DNA in serum samples. Results: The TTV genome was identified in 161 out of 236 (61.2%) healthy blood donors. The mean age for men and women was 43 and 57 years, respectively. Of the participants, 156 were male, and 107 were female. Donor age exhibited a significant association with virus presence (P=0.007); however, gender did not show a statistically significant association with the frequency of TTV infection in healthy blood donors (P=0.3). Conclusion: The study revealed a notably high frequency of the Torque teno virus in Yazd province, aligning with similar findings globally. Further investigations are warranted to elucidate the clinical implications of the virus in the healthy population.
背景:托克天奴病毒(TTV)是一种全球流行的人类病毒,但人们对其流行率、主要传播途径和发病机制的全面了解仍然有限。本研究旨在评估伊朗亚兹德健康献血者感染 TTV 的频率。材料和方法:共有 236 名健康献血者参与了 2015 年至 2016 年期间的研究,这些献血者均无 HIV/HBV/HCV 感染标记物。利用一套针对 5΄- UTR 区域的寡聚引物进行巢式聚合酶链反应(PCR),检测血清样本中的 TTV DNA。结果:在 236 名健康献血者中,有 161 人(61.2%)检测到了 TTV 基因组。男性和女性的平均年龄分别为 43 岁和 57 岁。其中男性 156 人,女性 107 人。献血者的年龄与病毒的存在有明显的关联(P=0.007);然而,性别与健康献血者感染 TTV 的频率在统计学上没有明显的关联(P=0.3)。结论研究显示,亚兹德省的托克-特诺病毒感染频率明显较高,这与全球的类似研究结果一致。有必要进行进一步调查,以阐明该病毒在健康人群中的临床影响。
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International journal of hematology-oncology and stem cell research
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