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  1. Article: Evidence Supporting a Phased Immuno-physiological Approach to COVID-19 From Prevention Through Recovery.

    Yanuck, S F / Pizzorno, J / Messier, H / Fitzgerald, K N

    Integrative medicine (Encinitas, Calif.)

    2020  Volume 19, Issue Suppl 1, Page(s) 8–35

    Abstract: This paper presents an evidence-based strategy for improving clinical outcomes in COVID-19. Recommendations are based on the phases of the disease, because optimal interventions for one phase may not be appropriate for a different phase. The four phases ... ...

    Abstract This paper presents an evidence-based strategy for improving clinical outcomes in COVID-19. Recommendations are based on the phases of the disease, because optimal interventions for one phase may not be appropriate for a different phase. The four phases addressed are: Prevention, Infection, Inflammation and Recovery. Underlying this phased approach is recognition of emerging evidence for two different components of pathophysiology, early infection and late stage severe complications. These two aspects of the disease suggest two different patterns of clinical emphasis that seem on the surface to be not entirely concordant. We describe the application of therapeutic strategies and appropriate tactics that address four main stages of disease progression for COVID-19. Emerging evidence in COVID-19 suggests that the SARS-CoV-2 virus may both evade the innate immune response and kill macrophages. Delayed innate immune response and a depleted population of macrophages can theoretically result in a blunted antigen presentation, delaying and diminishing activation of the adaptive immune response. Thus, one clinical strategy involves supporting patient innate and adaptive immune responses early in the time course of illness, with the goal of improving the timeliness, readiness, and robustness of both the innate and adaptive immune responses. At the other end of the disease pathology spectrum, risk of fatality in COVID-19 is driven by excessive and persistent upregulation of inflammatory mechanisms associated with cytokine storm. Thus, the second clinical strategy is to prevent or mitigate excessive inflammatory response to prevent the cytokine storm associated with high mortality risk. Clinical support for immune system pathogen clearance mechanisms involves obligate activation of immune response components that are inherently inflammatory. This puts the goals of the first clinical strategy (immune activation) potentially at odds with the goals of the second strategy(mitigation of proinflammatory effects). This creates a need for discernment about the time course of the illness and with that, understanding of which components of an overall strategy to apply at each phase of the time course of the illness. We review evidence from early observational studies and the existing literature on both outcomes and mechanisms of disease, to inform a phased approach to support the patient at risk for infection, with infection, with escalating inflammation during infection, and at risk of negative sequelae as they move into recovery.
    Keywords covid19
    Language English
    Publishing date 2020-04-17
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2100529-1
    ISSN 1945-7081 ; 1546-993X
    ISSN (online) 1945-7081
    ISSN 1546-993X
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Evidence Supporting a Phased Immuno-physiological Approach to COVID-19 From Prevention Through Recovery

    Yanuck, S. F. / Pizzorno, J. / Messier, H. / Fitzgerald, K. N.

    Integr Med (Encinitas)

    Abstract: This paper presents an evidence-based strategy for improving clinical outcomes in COVID-19 Recommendations are based on the phases of the disease, because optimal interventions for one phase may not be appropriate for a different phase The four phases ... ...

    Abstract This paper presents an evidence-based strategy for improving clinical outcomes in COVID-19 Recommendations are based on the phases of the disease, because optimal interventions for one phase may not be appropriate for a different phase The four phases addressed are: Prevention, Infection, Inflammation and Recovery Underlying this phased approach is recognition of emerging evidence for two different components of pathophysiology, early infection and late stage severe complications These two aspects of the disease suggest two different patterns of clinical emphasis that seem on the surface to be not entirely concordant We describe the application of therapeutic strategies and appropriate tactics that address four main stages of disease progression for COVID-19 Emerging evidence in COVID-19 suggests that the SARS-CoV-2 virus may both evade the innate immune response and kill macrophages Delayed innate immune response and a depleted population of macrophages can theoretically result in a blunted antigen presentation, delaying and diminishing activation of the adaptive immune response Thus, one clinical strategy involves supporting patient innate and adaptive immune responses early in the time course of illness, with the goal of improving the timeliness, readiness, and robustness of both the innate and adaptive immune responses At the other end of the disease pathology spectrum, risk of fatality in COVID-19 is driven by excessive and persistent upregulation of inflammatory mechanisms associated with cytokine storm Thus, the second clinical strategy is to prevent or mitigate excessive inflammatory response to prevent the cytokine storm associated with high mortality risk Clinical support for immune system pathogen clearance mechanisms involves obligate activation of immune response components that are inherently inflammatory This puts the goals of the first clinical strategy (immune activation) potentially at odds with the goals of the second strategy(mitigation of proinflammatory effects) This creates a need for discernment about the time course of the illness and with that, understanding of which components of an overall strategy to apply at each phase of the time course of the illness We review evidence from early observational studies and the existing literature on both outcomes and mechanisms of disease, to inform a phased approach to support the patient at risk for infection, with infection, with escalating inflammation during infection, and at risk of negative sequelae as they move into recovery
    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #32425712
    Database COVID19

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  3. Article: Expanding the neurological examination using functional neurologic assessment part I: methodological considerations.

    Motyka, T M / Yanuck, S F

    The International journal of neuroscience

    1999  Volume 97, Issue 1-2, Page(s) 61–76

    Abstract: Manual assessment of muscular function, in particular a method known as applied kinesiology (AK), is a clinical measure of neurologic function. A review of the literature reveals methodological problems with previous studies of AK as a form of neurologic ...

    Abstract Manual assessment of muscular function, in particular a method known as applied kinesiology (AK), is a clinical measure of neurologic function. A review of the literature reveals methodological problems with previous studies of AK as a form of neurologic assessment. Research designs that do not reflect clinical practice and principles of AK are common in the literature. Additional study is warranted to explore the potential of AK manual muscle testing as a diagnostic tool. We outline principles of AK and recommend that future research reflect more accurately the clinical practice of functional neurologic assessment and applied kinesiology.
    MeSH term(s) Humans ; Movement/physiology ; Neurologic Examination/methods
    Language English
    Publishing date 1999-12-01
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 3061-2
    ISSN 1543-5245 ; 0020-7454
    ISSN (online) 1543-5245
    ISSN 0020-7454
    DOI 10.3109/00207459908994303
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Expanding the neurological examination using functional neurologic assessment: part II neurologic basis of applied kinesiology.

    Schmitt, W H / Yanuck, S F

    The International journal of neuroscience

    1999  Volume 97, Issue 1-2, Page(s) 77–108

    Abstract: Functional Neurologic Assessment and treatment methods common to the practice of applied kinesiology are presented. These methods are proposed to enhance neurological examination and treatment procedures toward more effective assessment and care of ... ...

    Abstract Functional Neurologic Assessment and treatment methods common to the practice of applied kinesiology are presented. These methods are proposed to enhance neurological examination and treatment procedures toward more effective assessment and care of functional impairment. A neurologic model for these procedures is proposed. Manual assessment of muscular function is used to identify changes associated with facilitation and inhibition, in response to the introduction of sensory receptor-based stimuli. Muscle testing responses to sensory stimulation of known value are compared with usually predictable patterns based on known neuroanatomy and neurophysiology, guiding the clinician to an understanding of the functional status of the patient's nervous system. These assessment procedures are used in addition to other standard diagnostic measures to augment rather than replace the existing diagnostic armamentarium. The proper understanding of the neurophysiologic basis of muscle testing procedures will assist in the design of further investigations into applied kinesiology. Accordingly, the neurophysiologic basis and proposed mechanisms of these methods are reviewed.
    MeSH term(s) Gait/physiology ; Humans ; Mechanoreceptors/physiology ; Movement/physiology ; Muscle, Skeletal/physiology ; Muscle, Skeletal/physiopathology ; Neurologic Examination/methods
    Language English
    Publishing date 1999-12-01
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 3061-2
    ISSN 1543-5245 ; 0020-7454
    ISSN (online) 1543-5245
    ISSN 0020-7454
    DOI 10.3109/00207459908994304
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Applied Kinesiology-Forschung - eine Bestandsaufnahme

    Motyka, T.M. / Yanuck, S.F.

    Erfahrungsheilkunde

    2000  Volume 49, Issue 5, Page(s) 291

    Language German
    Document type Article
    ZDB-ID 500791-4
    ISSN 0014-0082
    Database Current Contents Medicine

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  6. Article: A mutant p53 tumor suppressor protein is a target for peptide-induced CD8+ cytotoxic T-cells.

    Yanuck, M / Carbone, D P / Pendleton, C D / Tsukui, T / Winter, S F / Minna, J D / Berzofsky, J A

    Cancer research

    1993  Volume 53, Issue 14, Page(s) 3257–3261

    Abstract: Cytotoxic T-lymphocytes (CTL) recognize processed peptide fragments of any endogenous protein, after these peptides are carried to the cell surface by class I major histocompatibility molecules. Thus, a tumor antigen does not have to be expressed as an ... ...

    Abstract Cytotoxic T-lymphocytes (CTL) recognize processed peptide fragments of any endogenous protein, after these peptides are carried to the cell surface by class I major histocompatibility molecules. Thus, a tumor antigen does not have to be expressed as an intact protein on the cell surface to be recognizable by CTL. However, mutant oncogene products have not yet been shown to be targets of CD8+ CTL. Here, we generate p53-specific CD8+ CTL by immunizing BALB/c mice with spleen cells pulsed with a peptide, corresponding to a 21-amino acid sequence encompassing a point mutation (135 Cys to Tyr) in the mutant p53 gene product from a human lung carcinoma. The mutation created a new Kd class I molecule binding motif sequence, and the determinant recognized was mapped to this motif and presented by the Kd class I molecule. The wild type peptide, without the mutation, was not recognized. Importantly, the CTL killed specifically BALB/c fibroblasts transfected with the mutant p53 gene and endogenously expressing the mutant protein, but not control fibroblasts or ones transfected with a different human mutant p53 gene. Thus, endogenously synthesized mutant p53, at levels found in tumors, can render cells targets for specific CTL, and these CTL can be generated by peptide immunization. These findings point the way toward an approach to selective immunotherapy against tumors.
    MeSH term(s) 3T3 Cells ; Amino Acid Sequence ; Animals ; Carcinoma, Non-Small-Cell Lung/genetics ; Epitopes/immunology ; Histocompatibility Antigens Class I/immunology ; Lung Neoplasms/genetics ; Mice ; Mice, Inbred BALB C ; Molecular Sequence Data ; Point Mutation ; T-Lymphocytes, Cytotoxic/immunology ; Tumor Suppressor Protein p53/genetics ; Tumor Suppressor Protein p53/immunology
    Chemical Substances Epitopes ; Histocompatibility Antigens Class I ; Tumor Suppressor Protein p53
    Language English
    Publishing date 1993-07-15
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 1432-1
    ISSN 1538-7445 ; 0008-5472
    ISSN (online) 1538-7445
    ISSN 0008-5472
    Database MEDical Literature Analysis and Retrieval System OnLINE

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