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  1. Article: Concurrent use of tumor necrosis factor inhibitor and tyrosine kinase inhibitor in ankylosing spondylitis and myeloid neoplasm.

    Gupta, Akash / Afinogenova, Yuliya / Podoltsev, Nikolai A / Danve, Abhijeet

    European journal of rheumatology

    2022  

    Abstract: Biologic disease-modifying agents (bDMARDs) are highly effective in controlling the symptoms of autoimmune rheumatic diseases. The decision on whether to continue bDMARDs following a cancer diagnosis can be challenging for patients and physicians. Here, ... ...

    Abstract Biologic disease-modifying agents (bDMARDs) are highly effective in controlling the symptoms of autoimmune rheumatic diseases. The decision on whether to continue bDMARDs following a cancer diagnosis can be challenging for patients and physicians. Here, we describe a case of a middle-aged male with ankylosing spondylitis who was controlled on infliximab (IFX) and found to have a myeloid neoplasm with Platelet-Derived Growth Factor Receptor Beta rearrangement. The patient was started on a tyrosine kinase inhibitor imatinib. Given its significant positive effect on patient's quality of life, IFX was continued with a favorable outcome. This case highlights the importance of shared decisionmaking in balancing risks and benefits of immunosuppressants in appropriate cases of hematologic malignancy.
    Language English
    Publishing date 2022-02-14
    Publishing country Turkey
    Document type Journal Article
    ZDB-ID 2873727-1
    ISSN 2148-4279 ; 2147-9720
    ISSN (online) 2148-4279
    ISSN 2147-9720
    DOI 10.5152/eurjrheum.2022.21097
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  2. Article ; Online: Update on gout management: what is old and what is new.

    Afinogenova, Yuliya / Danve, Abhijeet / Neogi, Tuhina

    Current opinion in rheumatology

    2021  Volume 34, Issue 2, Page(s) 118–124

    Abstract: Purpose of review: The global burden of gout is rising, as are the prevalence of associated comorbidities, all-cause mortality and societal costs. In this review, we discuss recent advances in epidemiology and treatment strategies for gout.: Recent ... ...

    Abstract Purpose of review: The global burden of gout is rising, as are the prevalence of associated comorbidities, all-cause mortality and societal costs. In this review, we discuss recent advances in epidemiology and treatment strategies for gout.
    Recent findings: Genetic factors and obesity are prominent contributors to hyperuricemia and gout, while dietary factors contribute to less variance in serum urate, though can still have some contribution to population attributable risk. A consensus statement by the Gout, Hyperuricemia and Crystal-Associated Disease Network outlined appropriate terminology regarding gout, which will aid in communication about various aspects of the disease. The 2020 American College of Rheumatology gout guideline offers comprehensive evidence-based recommendations for the management of hyperuricemia using urate-lowering therapy, prophylaxis when initiating urate-lowering therapy, treatment of gout flare and adjunctive management strategies. There is improved understanding of risk factors for allopurinol hypersensitivity syndrome and well tolerated use of allopurinol in chronic kidney disease. Trial data have provided new insights regarding cardiovascular risk with febuxostat. Several new drug therapies are being tested for both urate-lowering efficacy and gout flare management.
    Summary: Although there have been significant advances in understanding of risk factors and treatment approaches, gout remains suboptimally managed. There is substantial need for improving gout management efforts and gout education among patients and clinicians.
    MeSH term(s) Allopurinol/therapeutic use ; Febuxostat/therapeutic use ; Gout/drug therapy ; Gout/epidemiology ; Gout Suppressants/therapeutic use ; Humans ; Hyperuricemia/drug therapy ; Hyperuricemia/epidemiology ; Symptom Flare Up
    Chemical Substances Gout Suppressants ; Febuxostat (101V0R1N2E) ; Allopurinol (63CZ7GJN5I)
    Language English
    Publishing date 2021-12-09
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 1045317-9
    ISSN 1531-6963 ; 1040-8711
    ISSN (online) 1531-6963
    ISSN 1040-8711
    DOI 10.1097/BOR.0000000000000861
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  3. Article ; Online: Reply to "Increasing diversity in peanut oral immunotherapy research and accessibility".

    Soffer, Gary / Afinogenova, Yuliya / Factor, Jeffrey M

    The journal of allergy and clinical immunology. In practice

    2020  Volume 9, Issue 5, Page(s) 2133

    MeSH term(s) Allergens ; Arachis/immunology ; Desensitization, Immunologic ; Humans ; Immunotherapy ; Peanut Hypersensitivity/therapy ; Private Practice
    Chemical Substances Allergens
    Language English
    Publishing date 2020-09-25
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 2843237-X
    ISSN 2213-2201 ; 2213-2198
    ISSN (online) 2213-2201
    ISSN 2213-2198
    DOI 10.1016/j.jaip.2021.02.011
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  4. Article ; Online: IL-1 receptor 1 signaling shapes the development of viral antigen-specific CD4

    Park, Hong-Jai / Shin, Min Sun / Shin, Junghee J / Kim, Hyoungsu / Kang, Byunghyun / Par-Young, Jennefer / Unlu, Serhan / Afinogenova, Yuliya / Catanzaro, Jason / Young, Juan / Kim, Minhyung / Lee, Sang Jin / Jeon, Sangchoon / You, Sungyong / Racke, Michael K / Bucala, Richard / Kang, Insoo

    EBioMedicine

    2024  Volume 103, Page(s) 105114

    Abstract: Background: The innate immune cytokine interleukin (IL)-1 can affect T cell immunity, a critical factor in host defense. In a previous study, we identified a subset of human CD4: Methods: We characterized CD4: Findings: In healthy individuals, CD4! ...

    Abstract Background: The innate immune cytokine interleukin (IL)-1 can affect T cell immunity, a critical factor in host defense. In a previous study, we identified a subset of human CD4
    Methods: We characterized CD4
    Findings: In healthy individuals, CD4
    Interpretation: Our results demonstrate the significance of IL-1R1 expression in CD4
    Funding: Moderna to HJP, National Institutes of Health (NIH) 1R01AG056728 and R01AG055362 to IK and KL2 TR001862 to JJS, Quest Diagnostics to IK and RB, and the Mathers Foundation to RB.
    Language English
    Publishing date 2024-04-18
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2851331-9
    ISSN 2352-3964
    ISSN (online) 2352-3964
    DOI 10.1016/j.ebiom.2024.105114
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  5. Article: The efficacy and safety profile of albumin administration for patients with cirrhosis at high risk of hepatorenal syndrome is dose dependent.

    Afinogenova, Yuliya / Tapper, Elliot B

    Gastroenterology report

    2015  Volume 3, Issue 3, Page(s) 216–221

    Abstract: Background: Albumin is a critical component in the standard therapeutic approach to acute renal failure (ARF) and spontaneous bacterial peritonitis (SBP) in the setting of ascites. However, data regarding the safety and minimum effective dose are ... ...

    Abstract Background: Albumin is a critical component in the standard therapeutic approach to acute renal failure (ARF) and spontaneous bacterial peritonitis (SBP) in the setting of ascites. However, data regarding the safety and minimum effective dose are limited.
    Methods: We conducted a retrospective review of patients with decompensated cirrhosis who received albumin within the first 48 hours of hospitalization at Beth Israel Deaconess Medical Center between 2010 and 2013. Outcomes included 90-day risk of death or transplantation (primary) and (secondary) complications of albumin infusion (length of stay (LOS) and need for critical care)), all adjusted for comorbidity and severity of illness.
    Results: We included 169 patients with ARF and 88 patients with SBP. The optimal doses of albumin for a survival benefit were found to be 87.5 g and 100 g in the ARF and SBP cohorts, respectively. The odds ratio (OR) for the 90-day risk of death or liver transplantation associated with the optimal loading dose was 0.36 (95% CI: 0.17-0.76, P = 0.008) and 0.28 (95% CI: 0.07-0.97, P = 0.04) for the ARF and SBP cohorts, respectively. This effect persisted for patients with ARF who had neither hepatorenal syndrome (HRS) nor SBP (OR: 0.13, 95% CI: 0.007-0.79, P = 0.02). LOS (beta coefficient per log albumin dose: 1.69; 95% CI: 0.14-3.24, P = 0.03) and risk of critical care (OR/g albumin: 1.03; 95% CI: 1.01-1.05, P = 0.01) were also dose dependent.
    Conclusion: Albumin has a dose-dependent effect on both survival and complications in patients with cirrhosis with ARF (HRS and otherwise) and/or SBP.
    Language English
    Publishing date 2015-07-15
    Publishing country England
    Document type Journal Article
    ZDB-ID 2710871-5
    ISSN 2052-0034
    ISSN 2052-0034
    DOI 10.1093/gastro/gov032
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  6. Article ; Online: Use of Wireless Capsule Endoscopy for the Diagnosis and Grading of Esophageal Varices in Patients With Portal Hypertension: A Systematic Review and Meta-Analysis.

    McCarty, Thomas R / Afinogenova, Yuliya / Njei, Basile

    Journal of clinical gastroenterology

    2017  Volume 51, Issue 2, Page(s) 174–182

    Abstract: Introduction: Esophageal variceal bleeding is a severe complication of portal hypertension with significant morbidity and mortality. Although traditional screening and grading of esophageal varices has been performed by endogastroduodenoscopy (EGD), ... ...

    Abstract Introduction: Esophageal variceal bleeding is a severe complication of portal hypertension with significant morbidity and mortality. Although traditional screening and grading of esophageal varices has been performed by endogastroduodenoscopy (EGD), wireless video capsule endoscopy provides a minimally invasive alternative that may improve screening and surveillance compliance.
    Aim of the study: The aim of the study was to perform a systematic review and structured meta-analysis of all eligible studies to evaluate the efficacy of wireless capsule endoscopy for screening and diagnosis of esophageal varices among patients with portal hypertension.
    Methods: Searches of PubMed, EMBASE, Web of Science, and the Cochrane Library databases were performed through December 2015. Bivariate and hierarchical models were used to compute the pooled sensitivity and specificity, and to plot the summary receiver operating characteristics curve with summary point and corresponding 95% confidence region. Bias of included studies was assessed using the quality assessment of diagnostic accuracy studies-2.
    Results: Seventeen studies from 2005 to 2015 were included in this meta-analysis (n=1328). The diagnostic accuracy of wireless capsule endoscopy in the diagnosis of esophageal varices was 90% [95% confidence interval (CI), 0.88-0.93]. The diagnostic pooled sensitivity and specificity were 83% (95% CI, 0.76-0.89) and 85% (95% CI, 0.75-0.91), respectively. The diagnostic accuracy of wireless capsule endoscopy for the grading of medium to large varices was 92% (95% CI, 0.90-0.94). The pooled sensitivity and specificity were 72% (95% CI, 0.54-0.85) and 91% (95% CI, 0.86-0.94), respectively, for the grading of medium to large varices. The use of capsule demonstrated only mild adverse events. A sensitivity analysis limited to only high quality studies revealed similar results.
    Discussion: Wireless esophageal capsule endoscopy is well tolerated and safe in patients with liver cirrhosis and suspicion of portal hypertension. The sensitivity of capsule endoscopy is not currently sufficient to replace EGD as a first exploration in these patients, but given its high accuracy, it may have a role in cases of refusal or contraindication to EGD.
    Language English
    Publishing date 2017-02
    Publishing country United States
    Document type Journal Article
    ZDB-ID 448460-5
    ISSN 1539-2031 ; 0192-0790
    ISSN (online) 1539-2031
    ISSN 0192-0790
    DOI 10.1097/MCG.0000000000000589
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  7. Article ; Online: A distinct association of inflammatory molecules with outcomes of COVID-19 in younger versus older adults.

    Shin, Junghee J / Jeon, Sangchoon / Unlu, Serhan / Par-Young, Jennefer / Shin, Min Sun / Kuster, John K / Afinogenova, Yuliya / Kang, Yumi / Simonov, Michael / Buller, Gregory / Bucala, Richard / Kang, Insoo

    Clinical immunology (Orlando, Fla.)

    2021  Volume 232, Page(s) 108857

    Abstract: Aging can alter immunity affecting host defense. COVID-19 has the most devastating clinical outcomes in older adults, raising the implication of immune aging in determining its severity and mortality. We investigated biological predictors for clinical ... ...

    Abstract Aging can alter immunity affecting host defense. COVID-19 has the most devastating clinical outcomes in older adults, raising the implication of immune aging in determining its severity and mortality. We investigated biological predictors for clinical outcomes in a dataset of 13,642 ambulatory and hospitalized adult COVID-19 patients, including younger (age < 65, n = 566) and older (age ≥ 65, n = 717) subjects, with in-depth analyses of inflammatory molecules, cytokines and comorbidities. Disease severity and mortality in younger and older adults were associated with discrete immune mechanisms, including predominant T cell activation in younger adults, as measured by increased soluble IL-2 receptor alpha, and increased IL-10 in older adults although both groups also had shared inflammatory processes, including acute phase reactants, contributing to clinical outcomes. These observations suggest that progression to severe disease and death in COVID-19 may proceed by different immunologic mechanisms in younger versus older subjects and introduce the possibility of age-based immune directed therapies.
    MeSH term(s) Age Factors ; Aged ; Aging/metabolism ; Aging/pathology ; COVID-19/metabolism ; COVID-19/pathology ; Cytokines/metabolism ; Female ; Humans ; Inflammation/metabolism ; Inflammation/pathology ; Inflammation/virology ; Inflammation Mediators/metabolism ; Male ; Middle Aged ; Risk Factors ; SARS-CoV-2/pathogenicity ; Severity of Illness Index
    Chemical Substances Cytokines ; Inflammation Mediators
    Language English
    Publishing date 2021-09-22
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 1459903-x
    ISSN 1521-7035 ; 1521-6616
    ISSN (online) 1521-7035
    ISSN 1521-6616
    DOI 10.1016/j.clim.2021.108857
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  8. Article ; Online: Aberrant progranulin, YKL-40, cathepsin D and cathepsin S in Gaucher disease.

    Afinogenova, Yuliya / Ruan, Jiapeng / Yang, Ruhua / Kleytman, Nathaniel / Pastores, Gregory / Lischuk, Andrew / Mistry, Pramod K

    Molecular genetics and metabolism

    2019  Volume 128, Issue 1-2, Page(s) 62–67

    Abstract: In Gaucher disease, several macrophage-specific biomarkers have been validated for use in the clinic. However, Gaucher disease is more complex involving system-wide pathophysiology beyond the macrophage, and based on gene array analysis in our Gaucher ... ...

    Abstract In Gaucher disease, several macrophage-specific biomarkers have been validated for use in the clinic. However, Gaucher disease is more complex involving system-wide pathophysiology beyond the macrophage, and based on gene array analysis in our Gaucher disease mouse model and other emerging pathophysiologic insights, we evaluated serum levels of cathepsins D and S, YKL-40 and progranulin in Gaucher disease patients. We assessed their biomarker potential in Gaucher disease and compared them to established Gaucher disease biomarkers, chitotriosidase, chemokine ligand 18 (CCL18), and other indicators of disease severity and response to therapy. Mean YKL-40 and cathepsin D and S levels were significantly higher in Gaucher disease patients compared to healthy controls; in contrast, mean progranulin levels were lower in Gaucher disease patients compared to healthy controls. Enzyme replacement therapy resulted in a significant reversal of elevated cathepsin D and S but there was no change in progranulin and YKL-40 levels. Patients with persistent splenomegaly after long-term enzyme replacement therapy had significantly higher serum YKL-40 than patients with smaller spleens (63.0 ± 6.4 ng/ml vs. 46.4 ± 4.3 ng/ml, p = .03). Serum YKL-40 levels were higher in subjects with severe bone involvement (Hermann Score 3 to 5) compared to those with milder bone involvement (Hermann Score 1 to 2) (70.1 ± 4.3 ng/ml vs. 48.1 ± 3.7 ng/ml, p = .0002). YKL-40 was only weakly associated with chitotriosidase (r = 0.2, p = .008) and CCL18 (r = 0.3, p = .0004), and cathepsin S was moderately associated with chitotriosidase (r = 0.4, p = .01) and CCL18 (r = 0.6, p < .0001). Receiver operating curves for progranulin and YKL-40 demonstrated areas under the curves of 0.80 and 0.70, respectively. In conclusion, while these biomarkers do not meet robust properties of established macrophage-specific biomarkers, they may inform severity of skeletal disease, contribution of fibrosis to residual splenomegaly, and other disease manifestations. These findings, including markedly low progranulin levels that do not change upon enzyme replacement therapy, are intriguing to prompt further investigations to decipher their role in pathophysiology and relevance to diverse phenotypes of Gaucher disease.
    MeSH term(s) Adolescent ; Adult ; Aged ; Biomarkers/blood ; Cathepsin D/blood ; Cathepsins/blood ; Child ; Child, Preschool ; Chitinase-3-Like Protein 1/blood ; Cohort Studies ; Enzyme Replacement Therapy ; Gaucher Disease/blood ; Gaucher Disease/diagnosis ; Humans ; Middle Aged ; Progranulins/blood ; Splenomegaly/blood ; Young Adult
    Chemical Substances Biomarkers ; CHI3L1 protein, human ; Chitinase-3-Like Protein 1 ; Progranulins ; Cathepsins (EC 3.4.-) ; cathepsin S (EC 3.4.22.27) ; Cathepsin D (EC 3.4.23.5)
    Language English
    Publishing date 2019-07-23
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 1418518-0
    ISSN 1096-7206 ; 1096-7192
    ISSN (online) 1096-7206
    ISSN 1096-7192
    DOI 10.1016/j.ymgme.2019.07.014
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  9. Article ; Online: Defining Clinical and Immunological Predictors of Poor Immune Responses to COVID-19 mRNA Vaccines in Patients with Primary Antibody Deficiency.

    Shin, Junghee Jenny / Par-Young, Jennefer / Unlu, Serhan / McNamara, Andrew / Park, Hong-Jai / Shin, Min Sun / Gee, Renelle J / Doyle, Hester / Afinogenova, Yuliya / Zidan, Elena / Kwah, Jason / Russo, Armand / Mamula, Mark / Hsu, Florence Ida / Catanzaro, Jason / Racke, Michael / Bucala, Richard / Wilen, Craig / Kang, Insoo

    Journal of clinical immunology

    2022  Volume 42, Issue 6, Page(s) 1137–1150

    Abstract: Immune responses to coronavirus disease 2019 (COVID-19) mRNA vaccines in primary antibody deficiencies (PADs) are largely unknown. We investigated antibody and ... ...

    Abstract Immune responses to coronavirus disease 2019 (COVID-19) mRNA vaccines in primary antibody deficiencies (PADs) are largely unknown. We investigated antibody and CD4
    MeSH term(s) Antibodies, Viral ; CD8-Positive T-Lymphocytes ; COVID-19/prevention & control ; COVID-19 Vaccines ; Common Variable Immunodeficiency/diagnosis ; Humans ; Immunity, Cellular ; Immunoglobulin A ; Immunoglobulin G ; Primary Immunodeficiency Diseases ; RNA, Messenger ; SARS-CoV-2 ; Spike Glycoprotein, Coronavirus ; Vaccination ; Vaccines ; Vaccines, Synthetic ; mRNA Vaccines
    Chemical Substances Antibodies, Viral ; COVID-19 Vaccines ; Immunoglobulin A ; Immunoglobulin G ; RNA, Messenger ; Spike Glycoprotein, Coronavirus ; Vaccines ; Vaccines, Synthetic ; mRNA Vaccines ; spike protein, SARS-CoV-2
    Language English
    Publishing date 2022-06-17
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 779361-3
    ISSN 1573-2592 ; 0271-9142
    ISSN (online) 1573-2592
    ISSN 0271-9142
    DOI 10.1007/s10875-022-01296-4
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  10. Article ; Online: Community Private Practice Clinical Experience with Peanut Oral Immunotherapy.

    Afinogenova, Yuliya / Rubin, Tamar N / Patel, Sagar D / Powell, Rachel L / Gilo, Janina M / Denno, Morgan N / Soffer, Gary / Lee, Jason O / Mendelson, Louis M / Factor, Jeffrey M

    The journal of allergy and clinical immunology. In practice

    2020  Volume 8, Issue 8, Page(s) 2727–2735

    Abstract: Background: Peanut oral immunotherapy is an effective treatment for desensitizing peanut-allergic patients, but the frequency of adverse reactions has limited its widespread use.: Objective: To review the frequency of adverse reactions that patients ... ...

    Abstract Background: Peanut oral immunotherapy is an effective treatment for desensitizing peanut-allergic patients, but the frequency of adverse reactions has limited its widespread use.
    Objective: To review the frequency of adverse reactions that patients on peanut oral immunotherapy experience during build-up and maintenance phases and explore factors that may contribute to adverse events.
    Methods: A retrospective chart review of children and adults with peanut allergy undergoing peanut oral immunotherapy at the New England Food Allergy Treatment Center in West Hartford, Conn was performed. Data on patient demographics, allergic profile, peanut allergy testing, and details of reactions in build-up and maintenance phases were collected. A systemic reaction was defined as one of the following: (1) severe reaction involving 1 system, such as generalized hives and/or angioedema; (2) 2 or more of the following symptoms: cutaneous or oral, respiratory, or gastrointestinal symptoms; (3) drop in blood pressure; or (4) need for epinephrine.
    Results: Data were available on 783 patients aged 3.5 to 48.3 years. During buildup, 78 patients (10%) experienced at least 1 systemic reaction, 660 (84%) at least 1 gastrointestinal adverse event, 369 (47%) at least 1 cutaneous adverse event, and 157 (20%) at least 1 respiratory adverse event. Thirty-four patients (4%) required epinephrine during buildup. Six hundred ninety-seven patients (89%) completed buildup and progressed to maintenance. During maintenance, 131 patients (19%) experienced at least 1 systemic reaction, 190 (27%) at least 1 gastrointestinal adverse event, 104 (15%) at least 1 cutaneous adverse event, and 50 (7%) at least 1 respiratory adverse event. Seventy-four patients (11%) required epinephrine during maintenance. None of the adverse events required hospitalizations, and there were no mortalities. Nine patients (1%) were diagnosed with eosinophilic esophagitis during buildup or maintenance. Increasing pretreatment peanut specific IgE levels were associated with increased odds of a systemic reaction during buildup. Increasing age, pretreatment peanut specific IgE level, and a systemic reaction in buildup were associated with increased odds of a systemic reaction during maintenance.
    Conclusions: Peanut oral immunotherapy may be an effective and safe treatment for carefully selected peanut-allergic patients under the guidance of experienced providers. Specific patient characteristics and immunologic factors may help predict adverse events.
    MeSH term(s) Administration, Oral ; Adolescent ; Adult ; Allergens ; Arachis ; Child ; Child, Preschool ; Desensitization, Immunologic ; Humans ; Immunologic Factors ; Middle Aged ; Peanut Hypersensitivity/diagnosis ; Peanut Hypersensitivity/therapy ; Private Practice ; Retrospective Studies ; Young Adult
    Chemical Substances Allergens ; Immunologic Factors
    Language English
    Publishing date 2020-04-02
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2843237-X
    ISSN 2213-2201 ; 2213-2198
    ISSN (online) 2213-2201
    ISSN 2213-2198
    DOI 10.1016/j.jaip.2020.03.016
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