| Full text | |
| Author(s): Show less - |
Adriana da Silva Santos Duarte
[1]
;
Audrey Basso Zangirolami
[2]
;
Irene Santos
[3]
;
Fernanda Soares Niemann
[4]
;
Helen Naemi Honma
[5]
;
Emerson Clayton Amaro
[6]
;
Maurício Wesley Perroud Jr.
[7]
;
Fernando Vieira Pericole
[8]
;
Simone Cristina Olenscki Gilli
[9]
;
Bruno Deltreggia Benites
[10]
;
Sara Teresinha Olalla Saad
[11]
Total Authors: 11
|
| Affiliation: Show less - | [1] Universidade Estadual de Campinas. Centro de Hematologia e Hemoterapia - Brasil
[2] Universidade Estadual de Campinas. Centro de Hematologia e Hemoterapia - Brasil
[3] Universidade Estadual de Campinas. Centro de Hematologia e Hemoterapia - Brasil
[4] Universidade Estadual de Campinas. Centro de Hematologia e Hemoterapia - Brasil
[5] Universidade Estadual de Campinas. Faculdade de Ciências Médicas - Brasil
[6] Universidade Estadual de Campinas. Centro de Hematologia e Hemoterapia - Brasil
[7] Universidade Estadual de Campinas. Faculdade de Ciências Médicas - Brasil
[8] Universidade Estadual de Campinas. Centro de Hematologia e Hemoterapia - Brasil
[9] Universidade Estadual de Campinas. Centro de Hematologia e Hemoterapia - Brasil
[10] Universidade Estadual de Campinas. Centro de Hematologia e Hemoterapia - Brasil
[11] Universidade Estadual de Campinas. Centro de Hematologia e Hemoterapia - Brasil
Total Affiliations: 11
|
| Document type: | Journal article |
| Source: | Hematology, Transfusion and Cell Therapy; v. 46, n. 1, p. 30-35, 2024-05-27. |
| Abstract | |
Introduction Dendritic cell (DC) vaccines have demonstrated good efficacy in preventing relapse and in increasing survival of patients affected by a variety of both solid and hematological tumors. Most protocols used to generate these cells involve the automated separation of peripheral blood monocytes from patients. This approach requires specialized equipment, which elevates the cost of this type of therapy, potentially limiting the widespread access to patients. Method: In this study, we compare the yield and quality of dendritic cells generated from monocytes and isolated by an automated method or by manual methods using gradient centrifugation. Results The results demonstrate the equivalence of the 3 methods in relation to the yield and final quality of the product, however with considerable differences between the costs of these procedures. In addition, this study also demonstrates the feasibility of the antigenic pulse with autologous tumor cell lysates, constituting a source of antigens, not only easily obtained and manipulated, but also specific to the patient's tumor. Conclusion These findings may have important implications for emerging centers interested in using this medical approach and potentially increase the access of a greater number of patients to this therapeutic option. (AU) | |
| FAPESP's process: | 17/21801-2 - Predictors of severity and new treatments for bone marrow neoplasias |
| Grantee: | Sara Teresinha Olalla Saad |
| Support Opportunities: | Research Projects - Thematic Grants |