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  • 1
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2006
    In:  Neurology Vol. 66, No. 8 ( 2006-04-25), p. 1287-1287
    In: Neurology, Ovid Technologies (Wolters Kluwer Health), Vol. 66, No. 8 ( 2006-04-25), p. 1287-1287
    Type of Medium: Online Resource
    ISSN: 0028-3878 , 1526-632X
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2006
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  • 2
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 118, No. 12 ( 2021-03-23)
    Abstract: Pollen exposure weakens the immunity against certain seasonal respiratory viruses by diminishing the antiviral interferon response. Here we investigate whether the same applies to the pandemic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which is sensitive to antiviral interferons, if infection waves coincide with high airborne pollen concentrations. Our original hypothesis was that more airborne pollen would lead to increases in infection rates. To examine this, we performed a cross-sectional and longitudinal data analysis on SARS-CoV-2 infection, airborne pollen, and meteorological factors. Our dataset is the most comprehensive, largest possible worldwide from 130 stations, across 31 countries and five continents. To explicitly investigate the effects of social contact, we additionally considered population density of each study area, as well as lockdown effects, in all possible combinations: without any lockdown, with mixed lockdown−no lockdown regime, and under complete lockdown. We found that airborne pollen, sometimes in synergy with humidity and temperature, explained, on average, 44% of the infection rate variability. Infection rates increased after higher pollen concentrations most frequently during the four previous days. Without lockdown, an increase of pollen abundance by 100 pollen/m 3 resulted in a 4% average increase of infection rates. Lockdown halved infection rates under similar pollen concentrations. As there can be no preventive measures against airborne pollen exposure, we suggest wide dissemination of pollen−virus coexposure dire effect information to encourage high-risk individuals to wear particle filter masks during high springtime pollen concentrations.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
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    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2021
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  • 3
    In: Blood, American Society of Hematology, Vol. 110, No. 11 ( 2007-11-16), p. 4440-4440
    Abstract: Background: A systemic and intraventricular polychemotherapy regimen (“Bonn protocol”) with deferred radiotherapy had resulted in durable responses in 75% of patients 〈 60 years with primary CNS lymphoma (PCNSL), but had been complicated by a high rate of Ommaya reservoir infections. Purpose: Here, efficacy and toxicity of this regimen but without intraventricular treatment was evaluated in PCNSL. Patients and Methods : From 08/03 to 11/05, 18 patients with PCNSL 〈 60 years (median age 53 years) were treated within a phase II trial with a high-dose methotrexate (MTX; cycles 1,2,4 and 5) and cytarabine (Ara-C; cycles 3 and 6) based systemic therapy including dexamethasone, vinca-alkaloids, ifosfamide and cyclophosphamide. Results: Study accrual was prematurely stopped in 11/05 due to a high rate of early relapses. Seventeen/18 patients were assessable for response: Nine (53%) achieved complete response (CR), two (12%) complete response/unconfirmed (CRu), two (12%) partial response (PR), four (24%) showed progressive disease (PD); in one treatment was stopped due to toxicity. Median follow-up is 23 months; Kaplan-Meier estimates for median response duration were ten months only in responding patients and for median time to treatment failure (TTF) eight months in the whole group; median overall survival (OS) has not yet been reached. Systemic toxicity was mainly hematologic. Conclusions: In patients 〈 60 years with PCNSL polychemotherapy without intraventricular treatment results in a high response rate, but is associated with early relapses in the majority of cases. This is in contrast to the results achieved with the same protocol but with inclusion of intraventricular treatment.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
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    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2007
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  • 4
    In: Neuro-Oncology, Oxford University Press (OUP), Vol. 11, No. 1 ( 2009-02-01), p. 2-8
    Type of Medium: Online Resource
    ISSN: 1523-5866 , 1522-8517
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2009
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    detail.hit.zdb_id: 2094060-9
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  • 5
    In: Blood, American Society of Hematology, Vol. 112, No. 11 ( 2008-11-16), p. 3602-3602
    Abstract: Background: Data on relapsed central nervous system lymphoma (CNSL) is limited. Therefore, we have evaluated the clinical characteristics and outcome of relapsed CNSL patients at our centers. A central nervous system relapse is a serious complication of aggressive lymphomas. The prognosis is generally regarded as poor and standard therapies of relapsed CNSL have not yet been established. Patients and Methods: All pts with primary and secondary CNSL who were treated at Bonn University Hospital and Cologne University Hospital from 09/1995 – 12/2007 were included into the study. 125 pts could be identified; 102 with newly diagnosed primary CNSL (PCNSL) and 23 pts with secondary CNSL (SCNSL). First-line- treatment for pts with PCNSL consisted of high-dose methotrexate (MTX) in combination with vincristine, ifosfamide, prednisolone and cytarabine (Bonn protocol). Patients with SCNSL received a CHOP-like combination chemotherapy first-line. At cerebral relapse, for 17/23 pts SCNSL-treatment was Bonn polychemotherapy, 4/23 pts received an acute leukaemia regimen (GMALL-B-ALL protocol) at relapse and 2/23 received radiotherapy only. 81/125 pts (64%) were male with a median age of 62 yrs (range 27–77) and 72/125 pts (57%) were older 〉 60 years. Results: Overall response rate (CR+PR) was 63% (49CR +19PR) for PCNSL and 65% (12CR+3PR) for SCNSL. Median overall survival was 15.8 months for all 125 pts and 23 vs. 7.1 months for PCNSL and SCNSL. There was a difference in OS of 15 months between pts 〉 60 yrs (median 13 months) vs. pts 〈 60 yrs (median 28 months). After a median follow-up of 12 months (range 1–119) 80/125 (64%) pts with PCNSL and SCNSL relapsed (37) or progressed (43). All 80 patients relapsed/progressed again within the CNS. 65/80 pts initially suffered from PCNSL, 15/80 pts from SCNSL. Prognosis of relapsed/progressed PCNSL and SCNSL was dismal. 56/80 patients died. Median OS was short with only 8.5 months (range 1–124) survival time after relapse. Treatment at relapse was radiotherapy alone (16), radiotherapy in combination with temozolomide (2), radiotherapy in combination with MTX, dexamethasone and cytarabine (1), PVC-Chemotherapy (1), BEAM-Polychemothapy (1), Bonn polychemotherapy (7), cytarabine and etoposide (CYVE) with autologous stem cell transplantation (5) and “wait and see” (4). Response to relapse treatment was in 12 cases CR, in 9 cases PR and in 16 cases PD. Treatment at progress was radiotherapy alone (16), radiotherapy in combination with temozolomide (3), radiotherapy in combination with MTX, dexamethasone and cytarabine (1), BEAM-polychemotherapy (1), Bonn polychemotherapy (1), cytarabine and etoposide (CYVE) with autologous stem cell transplantation (2) and “wait and see”/no therapy (16). Response to progress treatment was in 3 cases CR, in 3 cases PR and in 37 cases PD. Conclusions: HD-MTX chemotherapy according to the Bonn Protocol is equally effective in PCNSL and SCNSL pts although the prognosis of pts with SCNSL seems to be worse. Prognosis of relapsed and refractory CNSL pts is dismal. Median OS was only 8.5 months. Therefore, new treatment strategies are urgently needed.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2008
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  • 6
    In: Development, The Company of Biologists, Vol. 135, No. 17 ( 2008-09-01), p. 2839-2843
    Abstract: Stem cells are maintained in an undifferentiated state by signals from their microenvironment, the stem cell niche. Despite its central role for organogenesis throughout the plant's life, little is known about how niche development is regulated in the Arabidopsis embryo. Here we show that, in the absence of functional ZWILLE (ZLL), which is a member of the ARGONAUTE (AGO) family, stem cell-specific expression of the signal peptide gene CLAVATA3 (CLV3) is not maintained despite increased levels of the homeodomain transcription factor WUSCHEL (WUS), which is expressed in the organising centre (OC) of the niche and normally promotes stem cell identity. Tissue-specific expression indicates that ZLLacts to maintain the stem cells from the neighbouring vascular primordium,providing direct evidence for a non-cell-autonomous mechanism. Furthermore,mutant and marker gene analyses suggest that during shoot meristem formation, ZLL functions in a similar manner but in a sequential order with its close homologue AGO1, which mediates RNA interference. Thus, WUS-dependent OC signalling to the stem cells is promoted by AGO1 and subsequently maintained by a provascular ZLL-dependent signalling pathway.
    Type of Medium: Online Resource
    ISSN: 1477-9129 , 0950-1991
    Language: English
    Publisher: The Company of Biologists
    Publication Date: 2008
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    SSG: 12
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  • 7
    In: Blood, American Society of Hematology, Vol. 112, No. 11 ( 2008-11-16), p. 3600-3600
    Abstract: Objectives: A pilot phase II trial was performed to evaluate response rate, response duration, overall survival, and toxicity in primary central nervous system lymphoma (PCNSL) after systemic and intraventricular chemotherapy with deferred radiotherapy. Patients and Methods: From 09/1995 to 12/2002, 65 patients with PCNSL (median age 62 years) were enrolled into a pilot/phase II study evaluating chemotherapy without radiotherapy. A high-dose methotrexate (MTX) (cycles 1,2,4,5) and cytarabine (ara-C) (cycles 3,6) based systemic therapy (including dexamethasone, vinca-alkaloids, ifosfamide and cyclophosphamide) was combined with intraventricular MTX, prednisolone and ara-C. Primary endpoint was time to treatment failure (TTF), secondary endpoints were response, overall survival, response duration, 5-year-survival fraction and (neuro)toxicity. Results: 34 patients were male, 31 female. Sixty-one of 65 patients were evaluable for response. Of these, 37 (61%) achieved a complete response (CR), 6 (10%) complete response/unconfirmed, and 12 (20%) progressed under therapy. Overall response rate was 71% for all patients and 86% for patients younger than 61 years. Six (9%) out of 65 patients died due to treatment-related complications. Follow-up time is 78 to 151 months in surviving patients (median 100 months). Kaplan Meier estimates for median time to treatment failure (TTF), median overall survival and median response duration are 22 months, 54 months and 37 months, respectively. For patients aged 60 years or older, the respective numbers were 7 months, 34 months and 30 months; in patients younger than 60 years, the Kaplan Meier estimate for TTF is 49 months, median overall survival and median response duration have not yet been reached. The 5-year survival fraction is 72% in patients 〈 60 years and 24% in older patients. Systemic toxicity was mainly hematologic. Ommaya reservoir infection occurred in 19% of the patients. At present, 17/30 (57%) of younger and 4/35 (9%) elderly patients are still alive. Only 5/30 (17%) of younger, but 19/35 (54%) of elderly patients received radiation salvage therapy at relapse. In 2/65 (3%), secondary cancers developed. In the subgroup of patients with long-term survival (n=17/30 under 61 years), 12 had an ongoing response, 1 an isolated CNS relapse (resolved by radiation), 1 an isolated ocular relapse (resolved by ocular radiation) and 3 a pure systemic relapse without CNS involvement (all resolved by systemic chemotherapy). Eleven of these 17 patients could be investigated by comprehensive neuropsychological testing, which revealed normal cognitive function in all of them. Conclusions: Primary chemotherapy based on high-dose MTX and ara-C is highly efficient in PCNSL. A substantial fraction of patients 〈 60 years can obviously be cured with this regimen.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2008
    detail.hit.zdb_id: 1468538-3
    detail.hit.zdb_id: 80069-7
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