血液科学(英文)Pub Date : 2022-07-14eCollection Date: 2022-07-01DOI: 10.1097/BS9.0000000000000130
Yongfei Hu, Yinglun Luo, Guangjue Tang, Yan Huang, Juanjuan Kang, Dong Wang
{"title":"Artificial intelligence and its applications in digital hematopathology.","authors":"Yongfei Hu, Yinglun Luo, Guangjue Tang, Yan Huang, Juanjuan Kang, Dong Wang","doi":"10.1097/BS9.0000000000000130","DOIUrl":"10.1097/BS9.0000000000000130","url":null,"abstract":"<p><p>The advent of whole-slide imaging, faster image data generation, and cheaper forms of data storage have made it easier for pathologists to manipulate digital slide images and interpret more detailed biological processes in conjunction with clinical samples. In parallel, with continuous breakthroughs in object detection, image feature extraction, image classification and image segmentation, artificial intelligence (AI) is becoming the most beneficial technology for high-throughput analysis of image data in various biomedical imaging disciplines. Integrating digital images into biological workflows, advanced algorithms, and computer vision techniques expands the biologist's horizons beyond the microscope slide. Here, we introduce recent developments in AI applied to microscopy in hematopathology. We give an overview of its concepts and present its applications in normal or abnormal hematopoietic cells identification. We discuss how AI shows great potential to push the limits of microscopy and enhance the resolution, signal and information content of acquired data. Its shortcomings are discussed, as well as future directions for the field.</p>","PeriodicalId":67343,"journal":{"name":"血液科学(英文)","volume":null,"pages":null},"PeriodicalIF":1.5,"publicationDate":"2022-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/33/7f/bs9-4-136.PMC9742095.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10712769","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
血液科学(英文)Pub Date : 2022-07-01DOI: 10.1097/BS9.0000000000000120
Xu Han, Peng Ji
{"title":"Carbon dots for the treatment of cancer-related anemia.","authors":"Xu Han, Peng Ji","doi":"10.1097/BS9.0000000000000120","DOIUrl":"10.1097/BS9.0000000000000120","url":null,"abstract":"","PeriodicalId":67343,"journal":{"name":"血液科学(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742109/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9795283","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
血液科学(英文)Pub Date : 2022-07-01DOI: 10.1097/BS9.0000000000000128
Jia Yu
{"title":"RNA and hematopoiesis.","authors":"Jia Yu","doi":"10.1097/BS9.0000000000000128","DOIUrl":"https://doi.org/10.1097/BS9.0000000000000128","url":null,"abstract":"Hematopoietic stem cells (HSCs) can differentiate into all mature functional blood cells via hematopoiesis","PeriodicalId":67343,"journal":{"name":"血液科学(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742080/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10712765","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
血液科学(英文)Pub Date : 2022-07-01DOI: 10.1097/BS9.0000000000000118
Robert Peter Gale
{"title":"Chimeric antigen receptor-T-cell therapy: China leading the way.","authors":"Robert Peter Gale","doi":"10.1097/BS9.0000000000000118","DOIUrl":"https://doi.org/10.1097/BS9.0000000000000118","url":null,"abstract":"","PeriodicalId":67343,"journal":{"name":"血液科学(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742101/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10712767","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
血液科学(英文)Pub Date : 2022-07-01DOI: 10.1097/BS9.0000000000000126
Hao Zhang, Guoyu Meng
{"title":"A typical bedside-to-bench investigation of leukemogenic driver MEF2D fusion reveals new targeted therapy in B-cell acute lymphoblastic leukemia.","authors":"Hao Zhang, Guoyu Meng","doi":"10.1097/BS9.0000000000000126","DOIUrl":"https://doi.org/10.1097/BS9.0000000000000126","url":null,"abstract":"<p><p>B-cell acute lymphoblastic leukemia (B-ALL) is a malignant tumor originating from B-lineage lymphoid precursor cells. The incidence of B-ALL is about 80% in childhood acute leukemia and 20% in adults. In recent years, with standardized treatment guided by risk stratification, the long-term disease-free survival rate of children is about 80%, while that of adults is less than 40%. However, the specific pathogenesis of the newly identified B-ALL and the targeted therapy strategies have not been vigorously investigated. In this review, we highlight the recent breakthroughs in mechanistic studies and novel therapeutic options in DUX4- and MEF2D-subtype B-ALLs.</p>","PeriodicalId":67343,"journal":{"name":"血液科学(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/87/ce/bs9-4-161.PMC9742090.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10731049","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
血液科学(英文)Pub Date : 2022-07-01DOI: 10.1097/BS9.0000000000000115
Ganiyu Olatunbosun Arinola, Elizabeth Disu, Adedokun Babatunde, Christopher Olopade, Olufunmilayo Olopade
{"title":"Assessment of humoral immunity and nutritionally essential trace elements in steady-state sickle cell disease Nigerian children before and after <i>Prevenar 13</i> pneumococcal vaccination.","authors":"Ganiyu Olatunbosun Arinola, Elizabeth Disu, Adedokun Babatunde, Christopher Olopade, Olufunmilayo Olopade","doi":"10.1097/BS9.0000000000000115","DOIUrl":"https://doi.org/10.1097/BS9.0000000000000115","url":null,"abstract":"<p><p>Children with sickle cell disease (SCD) are particularly prone to pneumococcal infection and administration of <i>Prevenar</i> 13 pneumococcal vaccine in Nigerian children with SCD is yet to be wide spread. This call for the need to study humoral immune responses stimulated by <i>Prevenar 13</i> pneumococcal vaccine in SCD children to confirm the benefit or otherwise for the use of <i>Prevenar 13</i> pneumococcal vaccine.</p><p><strong>Method: </strong>The levels of humoral (innate and adaptive) immune factors and associated nutritionally essential trace elements were determined following <i>Prevenar 13</i> pneumococcal vaccination of 23 Nigerian children with SCD. Serum innate humoral immune factors [Complement factors (C1q and C4), transferrin, ferritin, and C-reactive protein (CRP)] and adaptive humoral immune factors [IgG, IgA, IgM, and IgE] were determined using ELISA. Nutritionally essential trace elements such as iron (Fe), copper (Cu), and zinc (Zn) were measured also using an atomic absorption spectrophotometer.</p><p><strong>Results: </strong>The serum levels of certain innate humoral immune factors (ferritin, CRP, and C4), only one adaptive humoral immune factors (IgE), and essential trace elements (Fe, Zn, and Cu) were significantly elevated in children with SCD post <i>Prevenar 13</i> pneumococcal vaccination when compared to prevaccination levels.</p><p><strong>Conclusion: </strong>Vaccination of children with SCD with <i>Prevenar 13</i> pneumococcal vaccine was associated with increased levels of more innate humoral immune factors than adaptive factors. This study thus supports the administration of <i>Prevenar 13</i> pneumococcal vaccination to children with SCD.</p>","PeriodicalId":67343,"journal":{"name":"血液科学(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742099/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10706565","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
血液科学(英文)Pub Date : 2022-07-01DOI: 10.1097/BS9.0000000000000124
Li Han, Jianjun Chen, Rui Su
{"title":"Epitranscriptomics in myeloid malignancies.","authors":"Li Han, Jianjun Chen, Rui Su","doi":"10.1097/BS9.0000000000000124","DOIUrl":"https://doi.org/10.1097/BS9.0000000000000124","url":null,"abstract":"In eukaryotes, gene expression is highly orchestrated not only by genomic promoters and enhancers but also by covalent modifications added to either chromatin or RNAs. Traditionally, “epigenetics” refers to the chemical modifications that govern heritable changes in gene expression independent of the DNA sequence; “epitranscriptomics” indicates the covalent decorations in RNA, which plays a central role in posttranscriptional gene regulation. To date, >170 RNA chemical modifications have been characterized. Most of these modifications were originally identified in highly abundant noncoding RNA species, such as ribosomal RNAs (rRNAs), transfer RNAs (tRNAs), and small nuclear RNA (snRNAs). Recently, the substantial advances in high-throughput sequencing and analytical chemistry have enabled the precise detection and characterization of chemical modifications in messenger RNA (mRNA). Indeed, a consid- erable number of mRNA decorations have been documented, including N 6 -methyladenosine (m 6 A); N 1 -methyladenosine (m 1 A); N 6 ,2 ʹ -O-dimethyladenosine (m 6 A m ); 3-methylcytidine (m 3 C); 5-methylcytidine (m 5 C); 5-hydroxymethylcytidine (hm 5 C); N 4 -acetylcytidine (ac 4 C); Adenosine-to-inosine (A-to-I) editing; pseudouridine ( Ψ ); N 7 -methylguanosine (m 7 G) and 2 ʹ -O-methylated nucleotides (","PeriodicalId":67343,"journal":{"name":"血液科学(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742087/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10731043","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"KHSRP combines transcriptional and posttranscriptional mechanisms to regulate monocytic differentiation.","authors":"Jiayue Xu, Dongsheng Wang, Hongliu Ma, Xueying Zhai, Yue Huo, Yue Ren, Weiqian Li, Le Chang, Dongxu Lu, Yuehong Guo, Yanmin Si, Yufeng Gao, Xiaoshuang Wang, Yanni Ma, Fang Wang, Jia Yu","doi":"10.1097/BS9.0000000000000122","DOIUrl":"https://doi.org/10.1097/BS9.0000000000000122","url":null,"abstract":"<p><p>RNA-binding proteins (RBPs) are widely involved in the transcriptional and posttranscriptional regulation of multiple biological processes. The transcriptional regulatory ability of RBPs was indicated by the identification of chromatin-enriched RBPs (Che-RBPs). One of these proteins, KH-type splicing regulatory protein (KHSRP), is a multifunctional RBP that has been implicated in mRNA decay, alternative splicing, and miRNA biogenesis and plays an essential role in myeloid differentiation by facilitating the maturation of miR-129. In this study, we revealed that KHSRP regulates monocytic differentiation by regulating gene transcription and RNA splicing. KHSRP-occupied specific genomic sites in promoter and enhancer regions to regulate the expression of several hematopoietic genes through transcriptional activation and bound to pre-mRNA intronic regions to modulate alternative splicing during monocytic differentiation. Of note, KHSRP had co-regulatory effects at both the transcriptional and posttranscriptional levels on MOGOH and ADARB1. Taken together, our analyses revealed the dual DNA- and RNA-binding activities of KHSRP and have provided a paradigm to guide the analysis of other functional Che-RBPs in different biological systems.</p>","PeriodicalId":67343,"journal":{"name":"血液科学(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742092/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10731051","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
血液科学(英文)Pub Date : 2022-07-01DOI: 10.1097/BS9.0000000000000127
Mingzheng Hu, Yijie Wang, Jun Zhou
{"title":"Centrosome Defects in Hematological Malignancies: Molecular Mechanisms and Therapeutic Insights.","authors":"Mingzheng Hu, Yijie Wang, Jun Zhou","doi":"10.1097/BS9.0000000000000127","DOIUrl":"https://doi.org/10.1097/BS9.0000000000000127","url":null,"abstract":"<p><p>Defects in centrosomes are associated with a broad spectrum of hematological malignancies, such as leukemia and lymphoma. Centrosomes in these malignancies display both numerical and structural aberrations, including alterations in the number and size of centrioles, inappropriate post-translational modification of centrosomal proteins, and extra centrosome clustering. There is accumulating evidence that centrosome defects observed in hematological malignancies result from multiple factors, including dysregulation of the centrosome cycle and impairment of centriole biogenesis. In this review, we discuss the plausible mechanisms of centrosome defects and highlight their consequences in hematological malignancies. We also illustrate the latest therapeutic strategies against hematological malignancies by targeting centrosome anomalies.</p>","PeriodicalId":67343,"journal":{"name":"血液科学(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/aa/7c/bs9-4-143.PMC9742116.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10712766","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Risk factors for CMV infection within 100 days posttransplantation in patients with acute leukemia.","authors":"Juan Chen, Aiming Pang, Yuanqi Zhao, Li Liu, Runzhi Ma, Jialin Wei, Xin Chen, Yi He, Donglin Yang, Rongli Zhang, Weihua Zhai, Qiaoling Ma, Erlie Jiang, Mingzhe Han, Jiaxi Zhou, Sizhou Feng","doi":"10.1097/BS9.0000000000000121","DOIUrl":"https://doi.org/10.1097/BS9.0000000000000121","url":null,"abstract":"<p><p>To investigate the risk factors for cytomegalovirus (CMV) infection within 100 days and the relationship between early CMV infection and 1-year relapse for patients with acute leukemia following allogeneic hematopoietic stem cell transplantation (allo-HSCT).</p><p><strong>Methods: </strong>Three hundred fifty-nine patients with acute leukemia who received allo-HSCT at our center between January 2015 and January 2020 were retrospectively reviewed.</p><p><strong>Results: </strong>Of 359 patients, 48.19% (173) patients experienced CMV infection within 100 days posttransplantation. In univariate and multivariate logistic analysis, haploidentical-related donor (HRD) (<i>P</i> < 0.001; odds ratio [OR], 5.542; 95% confidence interval [CI], 3.186-9.639), and ratio of CD3<sup>+</sup>CD8<sup>+</sup> cells in lymphocytes <14.825% (<i>P</i> < 0.001; OR, 3.005; 95% CI, 1.712-5.275) were identified as 2 independent risk factors. One-year relapse rate (RR) between the CMV infection group and the non-CMV infection group was not statistically significant (18.5% vs 19.9%, <i>P</i> = 0.688). When we divided the total cohort into AML, ALL, and MAL subgroups, there were no significant differences as well (<i>P</i> = 0.138; <i>P</i> = 0.588; <i>P</i> = 0.117; respectively).</p><p><strong>Conclusion: </strong>In conclusion, donor type (HRD) and the insufficient recovery of CD3<sup>+</sup>CD8<sup>+</sup> cells were independent risk factors for CMV infection within 100 days posttransplantation in patients with acute leukemia. CMV infection within 100 days did not influence the incidence of relapse in 1 year for patients with acute leukemia.</p>","PeriodicalId":67343,"journal":{"name":"血液科学(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/39/84/bs9-4-164.PMC9742110.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10712771","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}