犬贫血性疾病输血疗法的疗效观察

输血疗法是救治动物的一项重要措施。为了验证输血疗法的作用,对数十例贫血病病犬进行输血疗法治疗,通过血常规检查、血液生化学检查等发现患犬均患有不同程度的贫血,红细胞数、血红蛋白含量、红细胞压积均明显低于正常值,在治疗原发病的同时配合了输血疗法。经过一段时间的治疗,发现应用输血疗法治疗的患犬痊愈快,患犬的红细胞数、血红蛋白含量、红细胞压积均逐渐升高接近正常值。由此可见,输血疗法对犬贫血病的治疗效果较好。     

Cytotoxic antibody in normal human serums reactive with tumor cells from acute lymphocytic leukemia

Serums showing complement-dependent cytotoxic reactions to acute lymphocytic leukemia cells were detected in three normal unimmunized subjects. These serums were reactive with tumor cells from 514 (514 tested) acute lymphocytic leukemia patients, and three (12 tested) patients with acute myelocytic leukemia; they did not react with tumor cells from patients with acute monocytic leukemia (two tested), with chronic lymphocytic leukemia (two tested) or with leukolymphosarcoma (two tested); nor did they react with normal lymphocytes from 52 different donors. These reactive serums appear to recognize antigens primarily associated with acute lymphocytic leukemia.     

Antigens specific for human lymphocytic and myeloid leukemia cells: detection by nonhuman primate antiserums

Primate antiserums to human leukemia cells can detect antigens specific for lymphocytic leukemia cells or antigens present on certain myeloid leukemia cells. The antigen specific for lymphocytic leukemia cells is destroyed by treatment with neuraminidase or trypsin. Tryptic digests of lymphocytic leukemia cells contain the antigen, which has a high molecular weight.     

Murine leukemia virus: restriction in fused permissive and nonpermissive cells

Cultures of human cells nonpermissive for mouse leukemia virus replication could not be induced to support virus replication by homologous fusion in the presence of Moloney leukemia virus. Human cells were also fused with permissive mouse cells, and the fate of the virus in heterokaryons was determined by a simultaneous autoradiography and fluorescent antibody technique. Heterokaryons containing the full chromosome complement of both cells were likewise nonpermissive for virus synthesis, but hybrids of human and mouse cells, which lacked up to half of the human chromosome complement, were permissive for virus synthesis. The results suggest that human cell genes can direct a repressive control over mouse leukemia virus replication.     

Antigen solubilized from human leukemia: lymphocyte stimulation

Soluble antigen was extracted with hypertonic (3 molar) potassium chloride from the malignant cells of seven patients with acute leukemia. The antigen and leukemia cells were used to stimulate autologous patients' and allogeneic normal donors' lymphocytes in mixed lymphocyte cultures. The lymphocytes of six patients showed significant blastogenic responses to autologous antigen. In contrast, the lymphocytes of only one of seven normal donors responded to the soluble antigens. Both patients' and normal subjects' lymphocytes responded to the intact leukemia cells. The use of these antigens should facilitate the study of specific tumor immunity in human leukemia.     

Detection of an antigen associated with acute leukemia

Antiserums to a purified cell membrane component from a Burkitt's lymphoma tissue culture cell line were produced in rabbits. These antiserums were cytotoxic to peripheral white blood cells from 8 of 15 patients with acute leukemia and 5 of 41 relatives, but not to peripheral white blood cells from leukemia patients in clinical remission or from normal individuals. These antiserums appear to be detecting an acute leukemia associated antigen or antigens.     

CD158受体表位封闭对急性髓系白血病患者NK细胞杀伤活性的影响

目的 研究急性髓系白血病患者NK细胞CD158受体表位封闭对自身白血病细胞杀伤活性的影响.方法 分离急性髓系白血病患者及健康志愿者外周血NK细胞,以自身白血病细胞及K562细胞为靶细胞,用CCK-8试剂盒检测CD158a、CD158b单克隆抗体封闭前后NK细胞在1：1、5：1、10：1效靶比下对靶细胞的杀伤活性.结果 患者与正常人NK细胞对K562细胞均有高度杀伤活性,且随效靶比增大而增高（P＜0.01）.效靶比为1：1、5：1、10：1时,患者NK胞在封闭前对白血病细胞杀伤活性分别为（1.5±0.3）%、（5.6±0.8）％、（11.8±0.6）%,封闭后分别为（21.8±0.7）％、（38.6±0.9）％、（53.9±1.4）％,各效靶比组封闭前后差异有统计学意义（P＜0.01）.结论 急性髓系白血病患者NK细胞CD158受体表位封闭可提高NK细胞对自身白血病细胞的体外杀伤能力.     

Viral infection across species barriers: reversible alteration of murine sarcoma virus for growth in cat cells

Infection of cat embryo cells by a centrifugally induced aggregate of murine sarcoma virus and feline leukemia virus gave rise to a defective, focus-forming virus which propagated in cat cells, but not in mouse cells. This virus, apparently enveloped with a feline leukemia virus coat, was later subjected to aggregation with murine leukemia virus, whereupon it regained the capacity for growth in mouse cells.     

Milk of dairy cows frequently contains a leukemogenic virus

Milk or viable milk cells collected from 24 dairy cattle naturally infected with bovine leukemia virus were inoculated into lambs, which were subsequently examined for the development of infection. With this bioassay, infectious virus was demonstrated in the milk of 17 of the cows. Bovine leukemia virus is leukemogenic in at least two mammalian species, is widespread in commercial dairy herds, and can infect a wide range of hosts in vivo and cells, including human cells, in vitro.     

Tuberculin hypersensitivity: studies with radioactive antigen and mononuclear cells

The type and fate of mononuclear cells of guinea pigs hypersensitive to tuberculin were studied by means of purified protein derivative labeled with I(125) and mononuclear cells labeled with tritiated thymidine. Purified protein derivative labeled with I(125) was taken up in vitro by lymphocytes and neutrophils from animals that were either sensitive or nonsensitive to tuberculin, but it was bound more frequently by the cells of sensitive animals. Passive transfer of tuberculin hypersensitivity by means of lymphocytes labeled with tritiated thymidine indicated that significant numbers of radioactive cells migrated to the site where the skin was tested with purified protein derivative only when the test was made immediately after transfusion. Although skin reactions from tests made with purified protein derivative 24 hours after transfusion were comparable to those from tests made immediately, the number of labeled cells at the sites of the later tests was not consistently larger than it was in controls (Histoplasmin reactions). Thus transfused tuberculin-sensitive cells are neither always attracted to the sites of the test with purified protein derivative nor are they required in large numbers at the site for a positive reaction to develop.     

Leukocyte alkaline phosphatase: electrophoretic variants associated with chronic myelogenous leukemia

Starch-gel electrophoresis of leukocyte alkaline phosphatases, rendered soluble by treating normal leukocytes with butanol, revealed three electrophoretic variants of the enzyme. The phosphatases in similarly prepared extracts of leukemia cells differed from the normal isozymes in electrophoretic. mobility. A single variant was detected in one case of untreated leukemia; a similar component and three additional ones were seen in leukemia treated with 6-mercaptopurine.     

Selective inhibition of leukemia cell proliferation by BCR-ABL antisense oligodeoxynucleotides

To determine the role of the BCR-ABL gene in the proliferation of blast cells of patients with chronic myelogenous leukemia, leukemia blast cells were exposed to synthetic 18-mer oligodeoxynucleotides complementary to two identified BCR-ABL junctions. Leukemia colony formation was suppressed, whereas granulocyte-macrophage colony formation from normal marrow progenitors was unaffected. When equal proportions of normal marrow progenitors and blast cells were mixed, exposed to the oligodeoxynucleotides, and assayed for residual colony formation, the majority of residual cells were normal. These findings demonstrate the requirement for a functional BCR-ABL gene in maintaining the leukemic phenotype and the feasibility of gene-targeted selective killing of neoplastic cells.     

Tumor cell rejection through terminal cell differentiation

Leukemic cells cultured in the presence of various conditioned media differentiate into macrophages. This finding suggested that the maintenance of undifferentiated state and self-renewal in vivo may be related to the inability of the host to generate an appropriate level of differentiation factor (DF). Evidence for this hypothesis was derived from experiments in vitro and in vivo with myeloid leukemia of rat. The following results were obtained: (i) in vitro, the percentage of cell differentiation at a fixed concentration of DF was inversely related to the concentration of cells; (ii) leukemic cell inoculates that were lethal to 7-day-old rats were rejected by 21-day-old rats; (iii) leukemic cells in diffusion chambers underwent differentiation in 21-day-old rats but not in 7-day-old rats; (iv) organs from 21-day-old rats contained more DF activity than those of 7-day-old rats; (v) treatment of rats with DF in diffusion chambers resulted in leukemic cell differentiation inside the chamber; and (vi) the development of leukemia in 7-day-old rats was aborted by treatment with DF. These results show that the differentiation of rat leukemia cells requires the appropriate level of DF. The proliferation of transplanted leukemia cells in 7-day-old rats goes unchecked because of inadequate generation of DF. Conversely, in the 21-day-old rats, rejection is accomplished by differentiation of the transplanted cells.     

Murine leukemia virus: high-frequency activation in vitro by 5-iododeoxyuridine and 5-bromodeoxyuridine

Cells of embryos of the high leukemic mouse strain AKR can be grown in culture as virus-negative cell lines. However, these lines and clonal sublines uniformly have the capacity to initiate synthesis of murine leukemia virus. Exposure of the cells to 5-iododeoxyuridine or 5-bromodeoxyuridine induced synthesis of virus in as high as 0.1 to 0.5 percent of the cells; many of the cells were producing virus as soon as 3 days after initiation of treatment. Induction of virus by these drugs is several orders of magnitude greater than that obtained with any other treatment tested. These studies indicate that the full genome of murine leukemia virus is present in an unexpressed form in all AKR cells and provide a potentially powerful technique for activating leukemia virus genomes in other cell systems.     

T-lymphocyte priming and protection against Friend leukemia by vaccinia-retrovirus env gene recombinant

The current prevalence of the acquired immune deficiency syndrome in humans has provoked renewed interest in methods of protective immunization against retrovirus-induced diseases. In this study, a vaccinia-retrovirus recombinant vector was constructed to study mechanisms of immune protection against Friend virus leukemia in mice. The envelope (env) gene from Friend murine leukemia virus (F-MuLV) was inserted into the genome of a vaccinia virus expression vector. Infected cells synthesized gp85, the glycosylated primary product of the env gene. Processing to gp70 and p15E, and cell surface localization, were similar to that occurring in cells infected with F-MuLV. Mice inoculated with live recombinant vaccinia virus had an envelope-specific T-cell proliferative response and, after challenge with Friend virus complex, developed neutralizing antibody and cytotoxic T cells (CTL) and were protected against leukemia. In contrast, unimmunized and control groups developed a delayed neutralizing antibody response, but no detectable CTL, and succumbed to leukemia. Genes of the major histocompatibility complex influenced protection induced by the vaccinia recombinant but not that induced by attenuated N-tropic Friend virus.     

短叶罗汉松叶结构的发育过程研究

短叶罗汉松叶的发育起始于茎端侧面分生组织区细胞分裂形成的叶原基。在叶的发育过程中,维管束下方的3个树脂道最先分化发育,然后,维管束内的原生木质部由近轴面向远轴面分化发育,同时原表皮下的一层薄壁细胞发育形成厚壁组织纤维,起支持幼叶的作用。当木质部基本成熟时,转输组织和韧皮部以及副转输组织开始发育,最后,叶肉组织分化发育为发达的栅栏组织细胞和海绵组织细胞。在叶内部结构分化发育的同时,表皮细胞的外侧形成较厚的角质层。在短叶罗汉松叶的结构中,发达的栅栏组织和角质层对于其生长在干旱和寒冷地区进行光合作用和蒸腾作用具有极为重要的意义。     

竹柏属和罗汉松属叶输导组织的观察(英文)

The conducting tissue structure of transverse and longitudinal sections was observed on leaves of Podocarpus and Nageia.Results showed:in Podocarpus leaves,there is only one midrib,the xylem tracheid of midrib vascular bundle is multi-form,transfusion tissue belongs to Cycas-type and transfusion tracheids are isodiametric,the accessory transfusion tracheids between palisade tissue and sponge tissue are developed;in Nageia leaves,there are plenty of parallel leaves,the xylem tracheids of each vein are relatively simple,transfusion tissue belongs to Taxus-type and transfusion tracheids are longer in longitudinal section than that in transverse section,the accessory transfusion tissue between palisade tissue and sponge tissue is absent.Considering other differences that in leaves of Podocarpus there are three resin ducts under vascular bundle of midrib,mesophyll cells are differentiated into palisade tissue and sponge tissue;in leaves of Nageia,there is only one resin duct under vascular bundle in each vein and no obvious differentiation in mesophyll cells,palisade tissue can be found on both sides,and sclereids can also be found in mesophyll tissue.The anatomical differences of leaf veins and mesophylls between Nageia and Podocarpus mentioned above support the viewpoint that Nageia and Podocarpus are two independent genera.     

HTLV-V: a new human retrovirus isolated in a Tac-negative T cell lymphoma/leukemia

A new human retrovirus was isolated from a continuous cell line derived from a patient with CD4+ Tac- cutaneous T cell lymphoma/leukemia. This virus is related to but distinct from human T cell leukemia/lymphoma virus types I and II (HTLV-I and HTLV-II) and human immunodeficiency virus (HIV-1). With the use of a fragment of provirus cloned from one patient with T cell leukemia, closely related sequences were found in DNA of the cell line and of tumor cells from seven other patients with the same disease; these sequences were only distantly related to HTLV-I. The phenotype of the cells and the clinical course of the disease were clearly distinguishable from leukemia associated with HTLV-I. All patients and the wife of one patient showed a weak serological cross-reactivity with both HTLV-I and HIV-1 antigens. None of the patients proved to be at any apparent risk for HIV-1 infection. The name proposed for this virus is HTLV-V, and the date indicate that it may be a primary etiological factor in the major group of cutaneous T cell lymphomas/leukemias, including the sporadic lymphomas known as mycoses fungoides.     

Conducting Tissue of Leaves in Nageia and Podocarpus

The conducting tissue structure of transverse and longitudinal sections was observed on leaves of Podocarpus and Nageia.Results showed:in Podocarpus leaves,there is only one midrib,the xylem tracheid of midrib vascular bundle is multi-form,transfusion tissue belongs to Cycas-type and transfusion tracheids are isodiametric,the accessory transfusion tracheids between palisade tissue and sponge tissue are developed;in Nageia leaves,there are plenty of parallel leaves,the xylem tracheids of each vein are relatively simple,transfusion tissue belongs to Taxus-type and transfusion tracheids are longer in longitudinal section than that in transverse section,the accessory transfusion tissue between palisade tissue and sponge tissue is absent.Considering other differences that in leaves of Podocarpus there are three resin ducts under vascular bundle of midrib,mesophyll cells are differentiated into palisade tissue and sponge tissue;in leaves of Nageia,there is only one resin duct under vascular bundle in each vein and no obvious differentiation in mesophyll cells,palisade tissue can be found on both sides,and sclereids can also be found in mesophyll tissue.The anatomical differences of leaf veins and mesophylls between Nageia and Podocarpus mentioned above support the viewpoint that Nageia and Podocarpus are two independent genera.     

竹柏属和罗汉松属叶输导组织的观察(英文)

The conducting tissue structure of transverse and longitudinal sections was observed on leaves of Podocarpus and Nageia.Results showed:in Podocarpus leaves,there is only one midrib,the xylem tracheid of midrib vascular bundle is multi-form,transfusion tissue belongs to Cycas-type and transfusion tracheids are isodiametric,the accessory transfusion tracheids between palisade tissue and sponge tissue are developed;in Nageia leaves,there are plenty of parallel leaves,the xylem tracheids of each vein are relatively simple,transfusion tissue belongs to Taxus-type and transfusion tracheids are longer in longitudinal section than that in transverse section,the accessory transfusion tissue between palisade tissue and sponge tissue is absent.Considering other differences that in leaves of Podocarpus there are three resin ducts under vascular bundle of midrib,mesophyll cells are differentiated into palisade tissue and sponge tissue;in leaves of Nageia,there is only one resin duct under vascular bundle in each vein and no obvious differentiation in mesophyll cells,palisade tissue can be found on both sides,and sclereids can also be found in mesophyll tissue.The anatomical differences of leaf veins and mesophylls between Nageia and Podocarpus mentioned above support the viewpoint that Nageia and Podocarpus are two independent genera.