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Article ; Online: Age, CD34+ cell dose, conditioning and pre-transplant cytopenias can help predict transfusion support in lymphoma patients undergoing autologous stem cell transplantation.

Regalado-Artamendi, Isabel / García-Fasanella, Marta / Medina, Laura / Fernandez-Sojo, Jesus / Esquirol, Albert / García-Cadenas, Irene / Martino, Rodrigo / Briones, Javier / Sierra, Jorge / Novelli, Silvana

Vox sanguinis

2023 Volume 118, Issue 8, Page(s) 681–689

Abstract: Background and objectives: Autologous stem cell transplant (ASCT) is a widely used therapy for lymphoma patients and can nowadays be performed on an outpatient basis. This study aimed to describe transfusion support in lymphoma patients undergoing ASCT ... ...

Abstract	Background and objectives: Autologous stem cell transplant (ASCT) is a widely used therapy for lymphoma patients and can nowadays be performed on an outpatient basis. This study aimed to describe transfusion support in lymphoma patients undergoing ASCT and identify increased or prolonged transfusion requirement predictors. Materials and methods: A retrospective study of all consecutive lymphoma patients undergoing ASCT between 2010 and 2020. Results: Out of 226 patients, 145 (64%) received red blood cell (RBC) transfusions, whereas all 226 (100%) required platelet transfusion (PT). Transfusions between Day +1 and +30 were higher in patients over 60 (2 [1-4] vs. 2 [0-2] RBC; p = 0.001 and 4 [2-8] vs. 3 [2-4] PT; p < 0.001); patients with pre-transplant anaemia (4 [2.5-6] vs. 2 [0-2] RBC; p < 0.001 and 5 [3-9] vs. 3 [2-4] PT; p = 0.001); pre-transplant thrombocytopenia (2 [1-4] vs. 2 [0-2] RBC; p < 0.001 and 4 [3-8.5] vs. 2 [1-3] PT; p < 0.001) or CD34 Conclusion: These four factors (age ≥60 years; BEAM conditioning, CD34
MeSH term(s)	Humans ; Middle Aged ; Hematopoietic Stem Cell Transplantation ; Retrospective Studies ; Transplantation, Autologous ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Lymphoma/therapy ; Lymphoma/etiology ; Stem Cell Transplantation ; Thrombocytopenia/etiology ; Anemia/therapy ; Anemia/etiology
Language	English
Publishing date	2023-06-25
Publishing country	England
Document type	Journal Article
ZDB-ID	80313-3
ISSN	1423-0410 ; 0042-9007
ISSN (online)	1423-0410
ISSN	0042-9007
DOI	10.1111/vox.13486
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Article ; Online: A hub-and-spoke model to deliver effective access to chimeric antigen receptor T-cell therapy in a public health network: the Catalan Blood and Tissue Bank experience.

Fernandez-Sojo, Jesus / Delgadillo, Joaquim / Vives, Joaquim / Rodriguez, Luciano / Mendoza, Ana / Azqueta, Carmen / Garcia-Buendia, Ana / Valdivia, Elena / Martorell, Lluis / Rubio-Lopez, Nuria / Linares, Mónica / Alonso, Sofia / Ancochea, Agueda / García-Rey, Enric / García-Muñoz, Nadia / Medina, Laura / Querol, Sergio

Cytotherapy

2022 Volume 25, Issue 1, Page(s) 14–19

Abstract: Background aims: To describe and analyze whether a hub-and-spoke organizational model could efficiently provide access to chimeric antigen receptor (CAR) T-cell therapy within a network of academic hospitals and address the growing demands of this ... ...

Abstract	Background aims: To describe and analyze whether a hub-and-spoke organizational model could efficiently provide access to chimeric antigen receptor (CAR) T-cell therapy within a network of academic hospitals and address the growing demands of this complex and specialized activity. Methods: The authors performed a retrospective evaluation of activity within the Catalan Blood and Tissue Bank network, which was established for hematopoietic stem cell transplantation to serve six CAR T-cell programs in academic hospitals of the Catalan Health Service. Procedures at six hospitals were followed from 2016 to 2021. Collection shipments of starting materials, CAR T-cell returns for storage and infusions for either clinical trials or commercial use were evaluated. Results: A total of 348 leukocytapheresis procedures were performed, 39% of which were delivered fresh and 61% of which were cryopreserved. The network was linked to seven advanced therapy medicinal product manufacturers. After production, 313 CAR T-cell products were shipped back to the central cryogenic medicine warehouse located in the hub. Of the units received, 90% were eventually administered to patients. A total of 281 patients were treated during this period, 45% in clinical trials and the rest with commercially available CAR T-cell therapies. Conclusions: A hub-and-spoke organizational model based on an existing hematopoietic stem cell transplantation program is efficient in incorporating CAR T-cell therapy into a public health hospital network. Rapid access and support of growing activity enabled 281 patients to receive CAR T cells during the study period.
MeSH term(s)	Humans ; Immunotherapy, Adoptive/methods ; Receptors, Chimeric Antigen ; Public Health ; Retrospective Studies ; Hematopoietic Stem Cell Transplantation ; Receptors, Antigen, T-Cell
Chemical Substances	Receptors, Chimeric Antigen ; Receptors, Antigen, T-Cell
Language	English
Publishing date	2022-08-27
Publishing country	England
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2039821-9
ISSN	1477-2566 ; 1465-3249
ISSN (online)	1477-2566
ISSN	1465-3249
DOI	10.1016/j.jcyt.2022.07.011
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Article ; Online: Development of an in-house bone marrow collection kit: The Catalan bone marrow transplantation group experience.

Vox sanguinis

2023 Volume 118, Issue 9, Page(s) 783–789

Abstract: Background and objectives: Bone marrow (BM) harvesting is one of the essential sources of stem cells for haematopoietic stem cell transplantation. In 2019, commercial BM collection kits became unavailable in Europe. Consequently, we created an in-house ... ...

Abstract	Background and objectives: Bone marrow (BM) harvesting is one of the essential sources of stem cells for haematopoietic stem cell transplantation. In 2019, commercial BM collection kits became unavailable in Europe. Consequently, we created an in-house BM collection kit as an alternative. Materials and methods: We compared two groups of BM collections. The first collections were taken using an in-house kit from June 2022 through February 2023 and the second with a commercial kit from February 2021 through May 2022. These all took place at seven collection centres (CC). We analysed the harvest quality (cell blood count, CD34+ cells, viability, potency and sterility), the incidents occurring with each kit and the time to neutrophil and platelet engraftment in recipients. Results: A total of 23 donors underwent BM harvesting with the in-house kit and 23 with the commercial one. Both cohorts were comparable regarding donor characteristics, CC and time to procedure. No statistical differences were found in harvest quality between the in-house and commercial kits. A new transfusion set was required in three BM harvests (13%) with the in-house kit because of filter clogging. The median time to neutrophil and platelet engraftment was 21 days for both cohorts and 29 days (in-house) and 33 days (commercial), p = 0.284, respectively. Conclusion: The in-house BM collection kit offers a real approach to solve the diminished supply of commercial kits. A higher risk of filter clogging was observed compared with commercial kits due to the lack of 850 and 500 μm filters.
MeSH term(s)	Humans ; Bone Marrow Transplantation/methods ; Bone Marrow ; Hematopoietic Stem Cell Transplantation ; Transplantation, Homologous ; Tissue Donors
Language	English
Publishing date	2023-08-02
Publishing country	England
Document type	Journal Article
ZDB-ID	80313-3
ISSN	1423-0410 ; 0042-9007
ISSN (online)	1423-0410
ISSN	0042-9007
DOI	10.1111/vox.13499
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Article ; Online: Acute liver failure due to immune-mediated hepatitis successfully managed with plasma exchange: New settings call for new treatment strategies?

Riveiro-Barciela, Mar / Muñoz-Couselo, Eva / Fernandez-Sojo, Jesús / Diaz-Mejia, Nely / Parra-López, Rafael / Buti, María

Journal of hepatology

2018 Volume 70, Issue 3, Page(s) 564–566

MeSH term(s)	Hepatitis ; Humans ; Immunotherapy ; Liver Failure, Acute ; Neoplasms ; Plasma Exchange
Language	English
Publishing date	2018-11-28
Publishing country	Netherlands
Document type	Letter ; Comment
ZDB-ID	605953-3
ISSN	1600-0641 ; 0168-8278
ISSN (online)	1600-0641
ISSN	0168-8278
DOI	10.1016/j.jhep.2018.10.020
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Article ; Online: Hemólisis intravascular por Clostridium perfringens.

Fernandez-Sojo, Jesús / Navarro, José Tomás / Vives-Polo, Susana / Juncà, Jordi

Medicina clinica

2014 Volume 142, Issue 1, Page(s) e1

Title translation	Clostridium perfringens-induced intravascular hemolysis.
MeSH term(s)	Aged ; Clostridium Infections/blood ; Clostridium perfringens ; Hemolysis ; Humans ; Male
Language	Spanish
Publishing date	2014-01-07
Publishing country	Spain
Document type	Case Reports ; Journal Article
ZDB-ID	411607-0
ISSN	1578-8989 ; 0025-7753
ISSN (online)	1578-8989
ISSN	0025-7753
DOI	10.1016/j.medcli.2013.05.031
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Article ; Online: Derrame pericárdico exudativo y oligoartritis en un paciente recién diagnosticado de síndrome mielodisplásico.

Fernández-Sojo, Jesús / Vives, Susana / Oliveras Vilà, Teresa / Ribera, Josep Maria

Medicina clinica

2014 Volume 143, Issue 1, Page(s) 43–44

Title translation	Exudative pericardial effusion and oligoarthritis in a patient newly diagnosed with myelodysplastic syndrome.
MeSH term(s)	Anemia, Refractory, with Excess of Blasts/complications ; Anemia, Refractory, with Excess of Blasts/diagnosis ; Anemia, Refractory, with Excess of Blasts/drug therapy ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Arthritis/drug therapy ; Arthritis/etiology ; Azacitidine/therapeutic use ; Cytarabine/administration & dosage ; Disease Progression ; Etoposide/administration & dosage ; Fatal Outcome ; Hepatomegaly/etiology ; Humans ; Idarubicin/administration & dosage ; Immunosuppressive Agents/therapeutic use ; Leukemia, Myeloid, Acute/drug therapy ; Leukemia, Myeloid, Acute/etiology ; Male ; Middle Aged ; Pericardial Effusion/drug therapy ; Pericardial Effusion/etiology ; Pleural Effusion/drug therapy ; Pleural Effusion/etiology ; Serositis/drug therapy ; Serositis/etiology
Chemical Substances	Immunosuppressive Agents ; Cytarabine (04079A1RDZ) ; Etoposide (6PLQ3CP4P3) ; Azacitidine (M801H13NRU) ; Idarubicin (ZRP63D75JW)
Language	Spanish
Publishing date	2014-07-07
Publishing country	Spain
Document type	Case Reports ; Letter
ZDB-ID	411607-0
ISSN	1578-8989 ; 0025-7753
ISSN (online)	1578-8989
ISSN	0025-7753
DOI	10.1016/j.medcli.2013.09.009
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Article ; Online: Estudio comparativo sobre la utilidad de la profilaxis antibacteriana con levofloxacino en pacientes receptores de un trasplante de progenitores hematopoyéticos.

Fernandez Sojo, Jesús / Batlle Massana, Montserrat / Morgades, Mireia / Vives Polo, Susana / Quesada, María Dolores / Ribera Santasusana, Josep María

Medicina clinica

2016 Volume 146, Issue 1, Page(s) 16–19

Abstract: Background: Bacterial infection remains a frequent complication in patients receiving a hematopoietic stem cell transplantation (HSCT). However, the impact of the antibacterial prophylaxis mortality in these patients is controversial.: Patients and ... ...

Title translation	Comparative study on the usefulness of antibacterial prophylaxis with levofloxacin in patients submitted to hematopoietic stem cell transplantation.
Abstract	Background: Bacterial infection remains a frequent complication in patients receiving a hematopoietic stem cell transplantation (HSCT). However, the impact of the antibacterial prophylaxis mortality in these patients is controversial. Patients and methods: Retrospective comparison of 2 consecutive groups of patients undergoing HSCT receiving (n=132) or not (n=107) antibacterial prophylaxis with levofloxacin. Results: 41% of patients receiving prophylaxis with levofloxacin had microbiologically documented infection (MDI) with bacteremia, compared with 40% of those not receiving levofloxacin. The frequency of gram-negative bacteremia was 11 and 38%, the resistance to levofloxacin was 39 and 14%, and the mortality was 8 and 7%, respectively. Conclusions: In our experience, the use of levofloxacin as prophylaxis in HSCT was associated with a lower frequency of gram-negative bacteremia but was not associated with a decreased rate of MDI and did not influence their outcome. In contrast, there was an increase in quinolone resistance in patients treated with levofloxacin.
MeSH term(s)	Adolescent ; Adult ; Aged ; Anti-Bacterial Agents/therapeutic use ; Antibiotic Prophylaxis ; Bacteremia/etiology ; Bacteremia/prevention & control ; Female ; Gram-Negative Bacterial Infections/etiology ; Gram-Negative Bacterial Infections/prevention & control ; Hematopoietic Stem Cell Transplantation/adverse effects ; Humans ; Levofloxacin/therapeutic use ; Male ; Middle Aged ; Retrospective Studies ; Treatment Outcome ; Young Adult
Chemical Substances	Anti-Bacterial Agents ; Levofloxacin (6GNT3Y5LMF)
Language	Spanish
Publishing date	2016-01-01
Publishing country	Spain
Document type	Comparative Study ; English Abstract ; Journal Article
ZDB-ID	411607-0
ISSN	1578-8989 ; 0025-7753
ISSN (online)	1578-8989
ISSN	0025-7753
DOI	10.1016/j.medcli.2015.05.019
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Article ; Online: Post thawing viable CD34+ Cells dose is a better predictor of clinical outcome in lymphoma patients undergoing autologous stem cell transplantation.

Fernandez-Sojo, Jesus / Cid, Joan / Azqueta, Carmen / Valdivia, Elena / Martorell, Lluis / Codinach, Margarita / Marsal, Julia / Mussetti, Alberto / Esquirol, Albert / Trabazo, Maria / Benitez, Maria Isabel / Ferra, Christelle / Fox, Maria Laura / Linares, Mónica / Alonso, Eva / García-Rey, Enric / García-Muñoz, Nadia / Medina, Laura / Castillo-Flores, Nerea /

Vall-Llovera, Ferran / Garcia, Antoni / Pinacho, Asuncion / Talarn, Carme / Arroba, Jose Garcia / Coll, Rosa / Santos, Mireia / Valero, Oliver / Carreras, Enric / Lozano, Miquel / Querol, Sergio

Bone marrow transplantation

2022 Volume 57, Issue 8, Page(s) 1341–1343

MeSH term(s)	Antigens, CD34 ; Hematopoietic Stem Cell Transplantation ; Humans ; Lymphoma/therapy ; Peripheral Blood Stem Cell Transplantation ; Transplantation, Autologous
Chemical Substances	Antigens, CD34
Language	English
Publishing date	2022-05-25
Publishing country	England
Document type	Letter
ZDB-ID	632854-4
ISSN	1476-5365 ; 0268-3369 ; 0951-3078
ISSN (online)	1476-5365
ISSN	0268-3369 ; 0951-3078
DOI	10.1038/s41409-022-01722-6
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Article ; Online: Leukocytapheresis variables and transit time for allogeneic cryopreserved hpc: better safe than sorry.

Fernandez-Sojo, Jesus / Horton, Roger / Cid, Joan / Azqueta, Carmen / Garcia-Buendia, Ana / Valdivia, Elena / Martorell, Lluis / Rubio-Lopez, Nuria / Codinach, Margarita / Aran, Gemma / Marsal, Julia / Mussetti, Alberto / Martino, Rodrigo / Diaz-de-Heredia, Cristina / Ferra, Christelle / Valcarcel, David / Linares, Mónica / Ancochea, Agueda / García-Rey, Enric /

García-Muñoz, Nadia / Medina, Laura / Carreras, Enric / Villa, Juliana / Lozano, Miquel / Gibson, Daniel / Querol, Sergio

Bone marrow transplantation

2022 Volume 57, Issue 10, Page(s) 1531–1538

Abstract: Cryopreservation was recommended to ensure continuity in allogeneic hematopoietic progenitor cells (HPC) transplantation during the COVID-19 pandemic. Several groups have shown no impact on clinical outcomes for patients who underwent HPC transplantation ...

Abstract	Cryopreservation was recommended to ensure continuity in allogeneic hematopoietic progenitor cells (HPC) transplantation during the COVID-19 pandemic. Several groups have shown no impact on clinical outcomes for patients who underwent HPC transplantation with cryopreserved products during the first months of this pandemic. However, concerns about quality control attributes after cryopreservation have been raised. We investigated, in 155 allogeneic peripheral blood cryopreserved HPC, leukocytapheresis characteristics influencing viable CD34
MeSH term(s)	Antigens, CD34/analysis ; COVID-19 ; Cell Survival ; Cryopreservation ; Hematopoietic Stem Cell Transplantation ; Hematopoietic Stem Cells ; Humans ; Leukapheresis ; Pandemics
Chemical Substances	Antigens, CD34
Language	English
Publishing date	2022-07-08
Publishing country	England
Document type	Journal Article
ZDB-ID	632854-4
ISSN	1476-5365 ; 0268-3369 ; 0951-3078
ISSN (online)	1476-5365
ISSN	0268-3369 ; 0951-3078
DOI	10.1038/s41409-022-01750-2
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Article ; Online: Latency reversal agents affect differently the latent reservoir present in distinct CD4+ T subpopulations.

Grau-Expósito, Judith / Luque-Ballesteros, Laura / Navarro, Jordi / Curran, Adrian / Burgos, Joaquin / Ribera, Esteban / Torrella, Ariadna / Planas, Bibiana / Badía, Rosa / Martin-Castillo, Mario / Fernández-Sojo, Jesús / Genescà, Meritxell / Falcó, Vicenç / Buzon, Maria J

PLoS pathogens

2019 Volume 15, Issue 8, Page(s) e1007991

Abstract: Latency reversal agents (LRAs) have proven to induce HIV-1 transcription in vivo but are ineffective at decreasing the size of the latent reservoir in antiretroviral treated patients. The capacity of the LRAs to perturb the viral reservoir present in ... ...

Abstract	Latency reversal agents (LRAs) have proven to induce HIV-1 transcription in vivo but are ineffective at decreasing the size of the latent reservoir in antiretroviral treated patients. The capacity of the LRAs to perturb the viral reservoir present in distinct subpopulations of cells is currently unknown. Here, using a new RNA FISH/flow ex vivo viral reactivation assay, we performed a comprehensive assessment of the viral reactivation capacity of different families of LRAs, and their combinations, in different CD4+ T cell subsets. We observed that a median of 16.28% of the whole HIV-reservoir induced HIV-1 transcripts after viral reactivation, but only 10.10% of these HIV-1 RNA+ cells produced the viral protein p24. Moreover, none of the LRAs were powerful enough to reactivate HIV-1 transcription in all CD4+ T cell subpopulations. For instance, the combination of Romidepsin and Ingenol was identified as the best combination of drugs at increasing the proportion of HIV-1 RNA+ cells, in most, but not all, CD4+ T cell subsets. Importantly, memory stem cells were identified as highly resistant to HIV-1 reactivation, and only the combination of Panobinostat and Bryostatin-1 significantly increased the number of cells transcribing HIV within this subset. Overall, our results validate the use of the RNA FISH/flow technique to assess the potency of LRAs among different CD4+ T cell subsets, manifest the intrinsic differences between cells that encompass the latent HIV reservoir, and highlight the difficulty to significantly impact the latent infection with the currently available drugs. Thus, our results have important implications for the rational design of therapies aimed at reversing HIV latency from diverse cellular reservoirs.
MeSH term(s)	Anti-HIV Agents/pharmacology ; CD4-Positive T-Lymphocytes/drug effects ; CD4-Positive T-Lymphocytes/immunology ; CD4-Positive T-Lymphocytes/virology ; Depsipeptides/pharmacology ; Diterpenes/pharmacology ; HIV Infections/drug therapy ; HIV Infections/immunology ; HIV Infections/virology ; HIV-1/drug effects ; HIV-1/immunology ; Humans ; Viral Load ; Virus Activation/drug effects ; Virus Activation/immunology ; Virus Latency/drug effects ; Virus Latency/immunology
Chemical Substances	Anti-HIV Agents ; Depsipeptides ; Diterpenes ; romidepsin (CX3T89XQBK) ; ingenol (IC77UZI9G8)
Language	English
Publishing date	2019-08-19
Publishing country	United States
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ZDB-ID	2205412-1
ISSN	1553-7374 ; 1553-7374
ISSN (online)	1553-7374
ISSN	1553-7374
DOI	10.1371/journal.ppat.1007991
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