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1.
EClinicalMedicine ; 39: 101086, 2021 Sep.
Article in English | MEDLINE | ID: mdl-34405140

ABSTRACT

BACKGROUND: Effective treatments are still needed to reduce the severity of symptoms, time of hospitalization, and mortality of COVID-19. SARS-CoV-2 specific memory T-lymphocytes obtained from convalescent donors recovered can be used as passive cell immunotherapy. METHODS: Between September and November 2020 a phase 1, dose-escalation, single centre clinical trial was conducted to evaluate the safety and feasibility of the infusion of CD45RA- memory T cells containing SARS-CoV-2 specific T cells as adoptive cell therapy against moderate/severe cases of COVID-19. Nine participants with pneumonia and/or lymphopenia and with at least one human leukocyte antigen (HLA) match with the donor were infused. The first three subjects received the lowest dose (1 × 105 cells/kg), the next three received the intermediate dose (5 × 105 cells/kg) and the last three received the highest dose (1 × 106 cells/kg) of CD45RA- memory T cells. Clinicaltrials.gov registration: NCT04578210. FINDINGS: All participants' clinical status measured by National Early Warning Score (NEWS) and 7-category point ordinal scales showed improvement six days after infusion. No serious adverse events were reported. Inflammatory parameters were stabilised post-infusion and the participants showed lymphocyte recovery two weeks after the procedure. Donor microchimerism was observed at least for three weeks after infusion in all patients. INTERPRETATION: This study provides preliminary evidence supporting the idea that treatment of COVID-19 patients with moderate/severe symptoms using convalescent CD45RA- memory T cells is feasible and safe. FUNDING: Clinical Trial supported by Spanish Clinical Research Network PT17/0017/0013. Co-funded by European Regional Development Fund/European Social Fund. CRIS CANCER Foundation Grant to AP-M and Agencia Valenciana de Innovación Grant AVI-GVA COVID-19-68 to BS.

2.
Front Cell Dev Biol ; 9: 620730, 2021.
Article in English | MEDLINE | ID: mdl-33718360

ABSTRACT

Syndrome coronavirus 2 (SARS-CoV-2) pandemic is causing a second outbreak significantly delaying the hope for the virus' complete eradication. In the absence of effective vaccines, we need effective treatments with low adverse effects that can treat hospitalized patients with COVID-19 disease. In this study, we determined the existence of SARS-CoV-2-specific T cells within CD45RA- memory T cells in the blood of convalescent donors. Memory T cells can respond quickly to infection and provide long-term immune protection to reduce the severity of COVID-19 symptoms. Also, CD45RA- memory T cells confer protection from other pathogens encountered by the donors throughout their life. It is of vital importance to resolve other secondary infections that usually develop in patients hospitalized with COVID-19. We found SARS-CoV-2-specific memory T cells in all of the CD45RA- subsets (CD3+, CD4+, and CD8+) and in the central memory and effector memory subpopulations. The procedure for obtaining these cells is feasible, easy to implement for small-scale manufacture, quick and cost-effective, involves minimal manipulation, and has no GMP requirements. This biobank of specific SARS-CoV-2 memory T cells would be immediately available "off-the-shelf" to treat moderate/severe cases of COVID-19, thereby increasing the therapeutic options available for these patients.

3.
Clin Transl Oncol ; 21(11): 1573-1577, 2019 Nov.
Article in English | MEDLINE | ID: mdl-30864020

ABSTRACT

BACKGROUND: Cutaneous squamous cell carcinoma (cSCC) is the leading cause of death in patients with recessive dystrophic epidermolysis bullosa (RDEB). We provide the management and prognosis of cSCC in RDEB patients at a Spanish reference center. MATERIALS AND METHODS: We retrospectively included patients with RDEB attended in La Paz University Hospital from November 1988 to October 2018. RESULTS: Fourteen patients developed at least one cSCC. Tumors were predominantly well differentiated. Nearly half of the tumors have recurred. Median time to first recurrence was 23.4 months (95% CI: 17.2-29.5). Five patients have developed distant metastases. Median overall survival (mOS) was 136.5 months since the diagnosis of the first cSCC (95% CI: 30.6-242.3). When distant metastases occurred, mOS was 6.78 months (95% CI: 1.94-11.61). CONCLUSIONS: cSCC is a life-threatening complication of RDEB patients. Although tumors are usually well differentiated, they tend to relapse. This is the first Spanish report of cSCC arising in RDEB patients.


Subject(s)
Carcinoma, Squamous Cell/etiology , Epidermolysis Bullosa Dystrophica/complications , Skin Neoplasms/etiology , Adolescent , Adult , Carcinoma, Squamous Cell/epidemiology , Carcinoma, Squamous Cell/mortality , Carcinoma, Squamous Cell/therapy , Epidermolysis Bullosa Dystrophica/mortality , Female , Humans , Lung Neoplasms/secondary , Male , Neoplasm Recurrence, Local , Prognosis , Retrospective Studies , Skin Neoplasms/epidemiology , Skin Neoplasms/mortality , Skin Neoplasms/therapy , Spain/epidemiology , Time Factors , Young Adult
4.
Int J Antimicrob Agents ; 52(5): 577-585, 2018 Nov.
Article in English | MEDLINE | ID: mdl-29969692

ABSTRACT

PURPOSE: There are few data in the literature regarding sepsis or septic shock due to extended-spectrum ß-lactamases (ESBL)-producing Enterobacteriaceae (E). The aim of this study was to assess predictors of outcome in septic patients with bloodstream infection (BSI) caused by ESBL-E. METHODS: Patients with severe sepsis or septic shock and BSI due to ESBL-E were selected from the INCREMENT database. The primary endpoint of the study was the evaluation of predictors of outcome after 30 days from development of severe sepsis or septic shock due to ESBL-E infection. Three cohorts were created for analysis: global, empirical-therapy and targeted-therapy cohorts. RESULTS: 367 septic patients were analysed. Overall mortality was 43.9% at 30 days. Escherichia coli (62.4%) and Klebsiella pneumoniae (27.2%) were the most frequent isolates. ß-lactam/ß-lactamase inhibitor (BLBLI) combinations were the most empirically used drug (43.6%), followed by carbapenems (29.4%). Empirical therapy was active in vitro in 249 (67.8%) patients, and escalation of antibiotic therapy was reported in 287 (78.2%) patients. Cox regression analysis showed that age, Charlson Comorbidity Index, McCabe classification, Pitt bacteremia score, abdominal source of infection and escalation of antibiotic therapy were independently associated with 30-day mortality. No differences in survival were reported in patients treated with BLBLI combinations or carbapenems in empirical or definitive therapy. CONCLUSIONS: BSI due to ESBL-E in patients who developed severe sepsis or septic shock was associated with high 30-day mortality. Comorbidities, severity scores, source of infection and antibiotic therapy escalation were important determinants of unfavorable outcome.


Subject(s)
Decision Support Techniques , Enterobacteriaceae Infections/diagnosis , Enterobacteriaceae Infections/mortality , Enterobacteriaceae/enzymology , Sepsis/diagnosis , Sepsis/mortality , beta-Lactamases/metabolism , Aged , Aged, 80 and over , Anti-Bacterial Agents/therapeutic use , Drug Therapy, Combination , Enterobacteriaceae/isolation & purification , Enterobacteriaceae Infections/drug therapy , Enterobacteriaceae Infections/microbiology , Female , Humans , Male , Middle Aged , Prognosis , Retrospective Studies , Sepsis/drug therapy , Sepsis/microbiology , Survival Analysis , Treatment Outcome , beta-Lactamase Inhibitors/therapeutic use , beta-Lactams/therapeutic use
9.
Clin Microbiol Infect ; 19(2): E72-9, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23231088

ABSTRACT

Bacteraemia due to carbapenemase-producing Enterobacteriaceae is an emerging medical problem. Management of this entity is complicated by the difficulty in identifying resistance patterns and the limited therapeutic options. A cohort study was performed including all episodes of bloodstream infection due to OXA-48-producing Enterobacteriaceae (O48PE), occurring between July 2010 and April 2012. Data on predisposing factors, clinical presentation, therapy and outcome were collected from medical records. There were 40 cases of bacteraemia caused by O48PE, 35 Klebsiella pneumoniae and five Escherichia coli. Patients were elderly with significant comorbidities (57.5% underlying malignancy). Thirty-five cases (87.5%) were nosocomial, and five (12.5%) were healthcare-associated. Patients had frequently been exposed to antibiotics and to invasive procedures during hospitalization. The most common source of bacteraemia was the urinary tract followed by deep intra-abdominal surgical site infection. Clinical presentation was severe sepsis or shock in 18 cases (45%). Extended-spectrum ß-lactamase production was detected in 92.5% of isolates. MIC(90) for ertapenem, imipenem and meropenem were 32, 16 and 16 mg/L, respectively. Most frequently preserved antibiotics were amikacin, colistin, tigecycline and fosfomycin. These antibiotics combined are the basis of targeted therapies, including carbapenem in selected cases. Median delay in starting clinically adequate and microbiologically appropriate treatment was 3 days. Crude mortality during admission and within 30 days from bacteraemia was 65% and 50%, respectively. Bloodstream infections caused by O48PE have a poor prognosis. Delay in diagnosis and in initiation of optimal antimicrobial therapy is frequent. Suspicion and rapid identification could contribute to improving outcomes.


Subject(s)
Bacteremia/epidemiology , Bacterial Proteins/metabolism , Escherichia coli Infections/epidemiology , Escherichia coli/enzymology , Klebsiella Infections/epidemiology , Klebsiella pneumoniae/enzymology , beta-Lactamases/metabolism , Adult , Age Factors , Aged , Aged, 80 and over , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/therapeutic use , Bacteremia/drug therapy , Bacteremia/microbiology , Bacteremia/pathology , Cross Infection/drug therapy , Cross Infection/epidemiology , Cross Infection/microbiology , Cross Infection/pathology , Escherichia coli/isolation & purification , Escherichia coli Infections/drug therapy , Escherichia coli Infections/microbiology , Escherichia coli Infections/pathology , Female , Humans , Klebsiella Infections/drug therapy , Klebsiella Infections/microbiology , Klebsiella Infections/pathology , Klebsiella pneumoniae/isolation & purification , Male , Microbial Sensitivity Tests , Middle Aged , Risk Factors , Treatment Outcome
10.
Eur J Clin Microbiol Infect Dis ; 30(12): 1497-502, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21556677

ABSTRACT

It is not known whether influenza-like illnesses (ILI) in pregnant women caused by influenza virus, specifically, those caused by the 2009 Influenza A H1N1 virus (nH1N1), can be clinically distinguished from those caused by other agents. From 1st July 2009 until 20th September 2009, an observational study including all pregnant women presenting at Hospital Universitario La Paz with an ILI was carried out. A specific reverse-transcriptase polymerase chain reaction (RT-PCR) for nH1N1 in nasopharyngeal swabs was prospectively carried out in all patients. Retrospectively, samples were analysed for multiple respiratory virus panel (RT-PCR microarray). Clinical, demographical and other microbiological variables were evaluated as well. A total of 45 pregnant women with ILI were admitted. Of these, 14 (31.1%) women had nH1N1 infection and 11 with a non-influenza ILI (35.48%) were positive for other viruses (five rhinovirus, four parainfluenza virus, one bocavirus and one adenovirus). In 20 patients, no aetiologic agent was identified. The clinical course of nH1N1 was mild, without deaths or severe complications. No significant differences were found when comparing the clinical presentation and course of patients with and without nH1N1 infection. Six women with nH1N1 infection received oseltamivir. Influenza and non-influenza ILI were clinically indistinguishable among pregnant women. Many ILI in pregnant women remain undiagnosed, despite undergoing an RT-PCR microarray for several respiratory viruses.


Subject(s)
Nasopharynx/virology , Pregnancy Complications, Infectious/epidemiology , Pregnancy Complications, Infectious/pathology , Virus Diseases/epidemiology , Virus Diseases/pathology , Viruses/classification , Viruses/isolation & purification , Adult , Female , Humans , Pregnancy , Pregnancy Complications, Infectious/virology , Prevalence , Retrospective Studies , Reverse Transcriptase Polymerase Chain Reaction , Virus Diseases/virology , Viruses/genetics
11.
Clin Microbiol Infect ; 17(6): 845-50, 2011 Jun.
Article in English | MEDLINE | ID: mdl-20673267

ABSTRACT

The first influenza pandemic in more than 40 years was declared in 2009. We aimed to evaluate the beliefs of Spanish infectious diseases professionals regarding several aspects of 2009 A (H1N1) influenza once the epidemic waned. An online survey was designed and distributed among members of the Spanish Society of Infectious Diseases and Clinical Microbiology (SEIMC). The survey considered hospital organization and preparedness planning and conduct, as well as the opinion of the infectious diseases professionals regarding several key issues. Between 7 March and 22 March 2010, 303 responses, corresponding to 12.8% of the SEIMC membership, were received. Of the respondents, 48.2% were microbiologists and 42.3% were clinicians dealing with infectious diseases. Forty-one per cent of respondents did not believe that 2009 A (H1N1) influenza had a more severe presentation than other seasonal influenzas. Only 5% fully agreed that 2009 A (H1N1) influenza had a more severe presentation. Influenza planning was available in 69.7% of represented institutions before the arrival of 2009 A (H1N1) influenza, and was considered to be useful, to different extents, by most professionals. In most institutions (88.3%), a multidisciplinary team was created to coordinate local pandemic influenza actions. The most successful protocols were those provided by regional healthcare authorities, followed by those from the CDC. The most problematic issues regarding 2009 A (H1N1) influenza were the management of patients in the emergency room and the vaccination and awareness of healthcare professionals (HCPs) regarding infection control. Microbiological diagnosis and the availability of antivirals were the least problematic areas. Although the majority of surveyed infectious diseases professionals did not believe that 2009 A (H1N1) influenza had an especially severe presentation, most of them agreed with the way that this epidemic was managed in their institutions.


Subject(s)
Communicable Disease Control/methods , Infection Control Practitioners , Influenza A Virus, H1N1 Subtype/isolation & purification , Influenza, Human/epidemiology , Influenza, Human/virology , Physicians , Antiviral Agents/administration & dosage , Antiviral Agents/supply & distribution , Cross Infection/prevention & control , Emergency Medical Services/methods , Health Facilities , Humans , Infection Control/methods , Influenza Vaccines/administration & dosage , Influenza Vaccines/supply & distribution , Influenza, Human/pathology , Influenza, Human/prevention & control , Spain/epidemiology
12.
Enferm Infecc Microbiol Clin ; 26 Suppl 8: 7-12, 2008 Jun.
Article in Spanish | MEDLINE | ID: mdl-19195432

ABSTRACT

Highly active antirretroviral therapy has transformed the prognosis of patient infected with human immunodeficiency virus. The efficacy of these drugs has shifted the clinicians; attention to other therapeutic aspects like QD regimens, fixed dose combinations and clinical safety. Tenofovir disoproxil fumarate(TDF) is a nucleoside monophosphate (nucleotide) analogue that inhibits reverse trascriptase enzyme. It's administered in a q.d. regimen and it's recommended by most of the clinical guidelines as a start regimen in combination with two other drugs. Currently more than 5 years of clinical experience is accumulated and confirmed that a combination of tenofovir and a nonnucleoside analogue transcriptase inhibitor is a comfortable, safe, highly effective and low pill burden regimen.


Subject(s)
Adenine/analogs & derivatives , Anti-HIV Agents/therapeutic use , HIV Infections/drug therapy , HIV Reverse Transcriptase/antagonists & inhibitors , HIV/drug effects , Organophosphonates/therapeutic use , Reverse Transcriptase Inhibitors/therapeutic use , Adenine/administration & dosage , Adenine/adverse effects , Adenine/chemistry , Adenine/pharmacology , Adenine/therapeutic use , Anti-HIV Agents/administration & dosage , Anti-HIV Agents/adverse effects , Anti-HIV Agents/chemistry , Anti-HIV Agents/classification , Anti-HIV Agents/pharmacology , Antiretroviral Therapy, Highly Active , Clinical Trials, Phase III as Topic/statistics & numerical data , Double-Blind Method , Drug Resistance, Multiple, Viral/genetics , Drug Therapy, Combination , HIV/enzymology , HIV/genetics , HIV Protease Inhibitors/administration & dosage , HIV Protease Inhibitors/adverse effects , HIV Protease Inhibitors/therapeutic use , HIV Reverse Transcriptase/genetics , Humans , Multicenter Studies as Topic , Organophosphonates/administration & dosage , Organophosphonates/adverse effects , Organophosphonates/chemistry , Organophosphonates/pharmacology , Patient Acceptance of Health Care , Practice Guidelines as Topic , Randomized Controlled Trials as Topic/statistics & numerical data , Reverse Transcriptase Inhibitors/administration & dosage , Reverse Transcriptase Inhibitors/adverse effects , Reverse Transcriptase Inhibitors/chemistry , Reverse Transcriptase Inhibitors/pharmacology , Tenofovir , Treatment Outcome
13.
Clin Transl Oncol ; 9(11): 742-3, 2007 Nov.
Article in English | MEDLINE | ID: mdl-18055330

ABSTRACT

Cerebral metastases from colorectal cancer occur in 8% of cases. Diagnosis is usually made when primary disease and widespread metastases are already known. However, the detection of brain metastases as the first sign of colorectal carcinoma without any liver and/or lung involvement is extremely rare. Central nervous system metastases are more commonly seen in rectal cancer and often occur concurrently with lung metastasis. We report a case of a patient with brain metastases as the first clinical manifestation of an adenocarcinoma of caecum without any other organ involvement.


Subject(s)
Adenocarcinoma/secondary , Brain Neoplasms/secondary , Colorectal Neoplasms/pathology , Adenocarcinoma/diagnosis , Aged , Aged, 80 and over , Brain Neoplasms/diagnosis , Humans , Male
14.
Clin. transl. oncol. (Print) ; 9(11): 742-743, nov. 2007.
Article in English | IBECS | ID: ibc-123385

ABSTRACT

Cerebral metastases from colorectal cancer occur in 8% of cases. Diagnosis is usually made when primary disease and widespread metastases are already known. However, the detection of brain metastases as the first sign of colorectal carcinoma without any liver and/or lung involvement is extremely rare. Central nervous system metastases are more commonly seen in rectal cancer and often occur concurrently with lung metastasis. We report a case of a patient with brain metastases as the first clinical manifestation of an adenocarcinoma of caecum without any other organ involvement (AU)


Subject(s)
Humans , Male , Female , Aged , Aged, 80 and over , Adenocarcinoma/diagnosis , Adenocarcinoma/secondary , Brain Neoplasms/diagnosis , Brain Neoplasms/secondary , Colorectal Neoplasms/pathology , Neoplasm Metastasis/diagnosis , Neoplasm Metastasis/physiopathology
20.
Med. integral (Ed. impr) ; 38(1): 8-17, jun. 2001. tab
Article in Es | IBECS | ID: ibc-15796

ABSTRACT

La anemia se define como la disminución de la concentración de hemoglobina por debajo de unos límites considerados normales para un determinado grupo de individuos de la misma edad, sexo y condiciones medioambientales. La existencia de un síndrome anémico es uno de los problemas diagnósticos más frecuentes en la práctica clínica y, en ocasiones, puede resultar una tarea difícil. Con este trabajo se pretende proporcionar unas pautas a seguir en el estudio del paciente anémico (AU)


Subject(s)
Female , Male , Humans , Anemia/diagnosis , Anemia/classification , Anemia/etiology , Anemia/therapy
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