Large scale isolation of human blood monocytes by continuous flow centrifugation leukapheresis and counterflow centrifugation elutriation for adoptive cellular immunotherapy in cancer patients. 1994

A Faradji, and A Bohbot, and M Schmitt-Goguel, and J C Siffert, and S Dumont, and M L Wiesel, and Y Piemont, and A Eischen, and J P Bergerat, and J Bartholeyns
Département d'Onco-Hématologie, Hôpitaux Universitaires de Strasbourg, France.

The increasing interest in mononuclear phagocytes for adoptive cellular immunotherapy (ACI) trials in cancer patients led us to define a procedural approach to harvest reproducibly highly purified single-cell suspensions of large numbers of functional human circulating blood monocytes (Mo). A semiclosed counterflow centrifugal elutriation (CCE) system has been developed, using a new large capacity Beckman JE 5.0 rotor with one interchangeable 40 ml or 5 ml separation chamber, to purify Mo from mononuclear cell (MNC) concentrates of healthy donors and cancer patients obtained by continuous flow centrifugation leukapheresis (CFCL). This method does not require a Ficoll density gradient centrifugation step. A total of 115 leukapheresis procedures were carried out in 35 patients and in 30 healthy donors by either Cobe 2997 or Cobe Spectra, with a similar efficiency in MNC apheresis. The average yield per leukapheresis procedure was 5.6 x 10(9) MNC of purity 90-100% (25-45% Mo, 40-65% lymphocytes). The average yields per elutriation procedure (R/O fraction) were 1.1 x 10(9) cells (purity 93% Mo) using the 5 ml separation chamber, and 1.5 x 10(9) cells (purity 91%) using the 40 ml separation chamber, with a respective recovery of 82 +/- 7% and 78 +/- 8% Mo. In vitro analysis of the viability and function of the purified Mo shows that neither morphological integrity nor physiological activity was compromised by this two-step isolation procedure, which additionally provides highly purified human Mo suspensions, in a quantity suitable for ACl of cancer patients.

UI MeSH Term Description Entries
D007111 Immunity, Cellular Manifestations of the immune response which are mediated by antigen-sensitized T-lymphocytes via lymphokines or direct cytotoxicity. This takes place in the absence of circulating antibody or where antibody plays a subordinate role. Cell-Mediated Immunity,Cellular Immune Response,Cell Mediated Immunity,Cell-Mediated Immunities,Cellular Immune Responses,Cellular Immunities,Cellular Immunity,Immune Response, Cellular,Immune Responses, Cellular,Immunities, Cell-Mediated,Immunities, Cellular,Immunity, Cell-Mediated,Response, Cellular Immune
D007116 Immunization, Passive Transfer of immunity from immunized to non-immune host by administration of serum antibodies, or transplantation of lymphocytes (ADOPTIVE TRANSFER). Convalescent Plasma Therapy,Immunoglobulin Therapy,Immunotherapy, Passive,Normal Serum Globulin Therapy,Passive Antibody Transfer,Passive Transfer of Immunity,Serotherapy,Passive Immunotherapy,Therapy, Immunoglobulin,Antibody Transfer, Passive,Passive Immunization,Therapy, Convalescent Plasma,Transfer, Passive Antibody
D007937 Leukapheresis The preparation of leukocyte concentrates with the return of red cells and leukocyte-poor plasma to the donor. Leukocytapheresis,Leukopheresis,Lymphapheresis,Lymphocytapheresis,Leukocytopheresis,Lymphocytopheresis,Lymphopheresis,Leukaphereses,Leukocytaphereses,Leukocytophereses,Leukophereses,Lymphaphereses,Lymphocytaphereses,Lymphocytophereses,Lymphophereses
D009000 Monocytes Large, phagocytic mononuclear leukocytes produced in the vertebrate BONE MARROW and released into the BLOOD; contain a large, oval or somewhat indented nucleus surrounded by voluminous cytoplasm and numerous organelles. Monocyte
D009369 Neoplasms New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms. Benign Neoplasm,Cancer,Malignant Neoplasm,Tumor,Tumors,Benign Neoplasms,Malignancy,Malignant Neoplasms,Neoplasia,Neoplasm,Neoplasms, Benign,Cancers,Malignancies,Neoplasias,Neoplasm, Benign,Neoplasm, Malignant,Neoplasms, Malignant
D002469 Cell Separation Techniques for separating distinct populations of cells. Cell Isolation,Cell Segregation,Isolation, Cell,Cell Isolations,Cell Segregations,Cell Separations,Isolations, Cell,Segregation, Cell,Segregations, Cell,Separation, Cell,Separations, Cell
D002470 Cell Survival The span of viability of a cell characterized by the capacity to perform certain functions such as metabolism, growth, reproduction, some form of responsiveness, and adaptability. Cell Viability,Cell Viabilities,Survival, Cell,Viabilities, Cell,Viability, Cell
D002498 Centrifugation Process of using a rotating machine to generate centrifugal force to separate substances of different densities, remove moisture, or simulate gravitational effects. It employs a large motor-driven apparatus with a long arm, at the end of which human and animal subjects, biological specimens, or equipment can be revolved and rotated at various speeds to study gravitational effects. (From Websters, 10th ed; McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D016219 Immunotherapy, Adoptive Form of adoptive transfer where cells with antitumor activity are transferred to the tumor-bearing host in order to mediate tumor regression. The lymphoid cells commonly used are lymphokine-activated killer (LAK) cells and tumor-infiltrating lymphocytes (TIL). This is usually considered a form of passive immunotherapy. (From DeVita, et al., Cancer, 1993, pp.305-7, 314) Adoptive Cellular Immunotherapy,Adoptive Immunotherapy,CAR T-Cell Therapy,Cellular Immunotherapy, Adoptive,Chimeric Antigen Receptor Therapy,Immunotherapy, Adoptive Cellular,Adoptive Cellular Immunotherapies,Adoptive Immunotherapies,CAR T Cell Therapy,CAR T-Cell Therapies,Cellular Immunotherapies, Adoptive,Immunotherapies, Adoptive,Immunotherapies, Adoptive Cellular,T-Cell Therapies, CAR,T-Cell Therapy, CAR,Therapies, CAR T-Cell,Therapy, CAR T-Cell

Related Publications

A Faradji, and A Bohbot, and M Schmitt-Goguel, and J C Siffert, and S Dumont, and M L Wiesel, and Y Piemont, and A Eischen, and J P Bergerat, and J Bartholeyns
January 1979, Transfusion,
A Faradji, and A Bohbot, and M Schmitt-Goguel, and J C Siffert, and S Dumont, and M L Wiesel, and Y Piemont, and A Eischen, and J P Bergerat, and J Bartholeyns
November 1978, Experimental hematology,
A Faradji, and A Bohbot, and M Schmitt-Goguel, and J C Siffert, and S Dumont, and M L Wiesel, and Y Piemont, and A Eischen, and J P Bergerat, and J Bartholeyns
July 1982, Blood,
A Faradji, and A Bohbot, and M Schmitt-Goguel, and J C Siffert, and S Dumont, and M L Wiesel, and Y Piemont, and A Eischen, and J P Bergerat, and J Bartholeyns
September 1986, Journal of immunological methods,
A Faradji, and A Bohbot, and M Schmitt-Goguel, and J C Siffert, and S Dumont, and M L Wiesel, and Y Piemont, and A Eischen, and J P Bergerat, and J Bartholeyns
August 1982, American journal of veterinary research,
A Faradji, and A Bohbot, and M Schmitt-Goguel, and J C Siffert, and S Dumont, and M L Wiesel, and Y Piemont, and A Eischen, and J P Bergerat, and J Bartholeyns
May 1984, The Journal of laboratory and clinical medicine,
A Faradji, and A Bohbot, and M Schmitt-Goguel, and J C Siffert, and S Dumont, and M L Wiesel, and Y Piemont, and A Eischen, and J P Bergerat, and J Bartholeyns
August 1980, Cellular immunology,
A Faradji, and A Bohbot, and M Schmitt-Goguel, and J C Siffert, and S Dumont, and M L Wiesel, and Y Piemont, and A Eischen, and J P Bergerat, and J Bartholeyns
September 1983, Journal of immunological methods,
A Faradji, and A Bohbot, and M Schmitt-Goguel, and J C Siffert, and S Dumont, and M L Wiesel, and Y Piemont, and A Eischen, and J P Bergerat, and J Bartholeyns
September 1983, Journal of immunological methods,
A Faradji, and A Bohbot, and M Schmitt-Goguel, and J C Siffert, and S Dumont, and M L Wiesel, and Y Piemont, and A Eischen, and J P Bergerat, and J Bartholeyns
January 1991, Haematologica,
Copied contents to your clipboard!