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2.
Hum Immunol ; 80(6): 385-392, 2019 Jun.
Article in English | MEDLINE | ID: mdl-30836129

ABSTRACT

Vascularized composite allotransplantation (VCA) has emerged as the most recent field of transplantation to offer an alternative treatment for those patients that have failed or are not suitable candidates for conventional therapy. Most of the current clinical experience in this field is with recipients of skin containing grafts such as the face, upper extremity and abdominal wall transplants. Like solid organ recipients, VCA recipients require lifelong systematic immunosuppression to maintain their grafts. To date, the most successful immunosuppressant regimens are calcineurin inhibitor based and have been targeted to the control of T cells. While these regimens have resulted in excellent short term graft survival in solid organ transplantation, achieving significant improvements in long term survival has been more challenging. The reasons are multi-factorial, but a role for B cells and humoral immunity has been proposed. Antibody mediated rejection leading to chronic rejection has been cited as the leading cause of renal graft loss. While the number of VCA transplants performed is still small, evidence to date suggests that antibody mediated rejection may occur less frequently than seen in solid organ transplants. Here we will discuss the role of B cell immunity in solid organ transplantation as it pertains and contrasts to the field of VCA and present some examples of possible sequela of B cell immunity in a series of hand transplant recipients.


Subject(s)
B-Lymphocytes/immunology , Graft Rejection/immunology , Graft Survival , Immunity, Humoral , Vascularized Composite Allotransplantation , Animals , Hand Transplantation , Humans , Immune Tolerance , Transplantation Immunology
4.
Reprod Biol Endocrinol ; 12: 50, 2014 Jun 13.
Article in English | MEDLINE | ID: mdl-24927773

ABSTRACT

Endometriosis is a common and painful condition affecting women of reproductive age. While the underlying pathophysiology is still largely unknown, much advancement has been made in understanding the progression of the disease. In recent years, a great deal of research has focused on non-invasive diagnostic tools, such as biomarkers, as well as identification of potential therapeutic targets. In this article, we will review the etiology and cellular mechanisms associated with endometriosis as well as the current diagnostic tools and therapies. We will then discuss the more recent genomic and proteomic studies and how these data may guide development of novel diagnostics and therapeutics. The current diagnostic tools are invasive and current therapies primarily treat the symptoms of endometriosis. Optimally, the advancement of "-omic" data will facilitate the development of non-invasive diagnostic biomarkers as well as therapeutics that target the pathophysiology of the disease and halt, or even reverse, progression. However, the amount of data generated by these types of studies is vast and bioinformatics analysis, such as we present here, will be critical to identification of appropriate targets for further study.


Subject(s)
Endometriosis/physiopathology , Animals , Apoptosis , Biomarkers/metabolism , Cell Proliferation , Computational Biology/methods , Disease Progression , Endometriosis/diagnosis , Endometriosis/metabolism , Endometriosis/therapy , Female , Humans , Infertility, Female/etiology , Infertility, Female/prevention & control , Neovascularization, Pathologic , Signal Transduction
5.
Clin Biochem ; 47(10-11): 983-7, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24560655

ABSTRACT

The transgender community is arguably the most marginalized and underserved population in medicine. A special issue focusing on men's health would be incomplete without mention of this vulnerable population, which includes those transitioning to and from the male gender. Transgender patients face many barriers in their access to healthcare including historical stigmatization, both structural and financial barriers, and even a lack of healthcare provider experience in treating this unique population. Historical stigmatization fosters a reluctance to disclose gender identity, which can have dire consequences for long-term outcomes due to a lack of appropriate medical history including transition-related care. Even if a patient is willing to disclose their gender identity and transition history, structural barriers in current healthcare settings lack the mechanisms necessary to collect and track this information. Moreover, healthcare providers acknowledge that information is lacking regarding the unique needs and long-term outcomes for transgender patients, which contributes to the inability to provide appropriate care. All of these barriers must be recognized and addressed in order to elevate the quality of healthcare delivered to the transgender community to a level commensurate with the general population. Overcoming these barriers will require redefinition of our current system such that the care a patient receives is not exclusively linked to their sex but also considers gender identity.


Subject(s)
Delivery of Health Care , Quality of Health Care , Transgender Persons , Female , Humans , Male
6.
Am J Med ; 127(2): 159-62, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24332725

ABSTRACT

BACKGROUND: Clinical guidelines recommend laboratory monitoring of transgender persons on cross-sex hormone therapy, but gender-specific reference intervals leave clinicians with the dilemma of deciding what is "normal" for each patient. The goal of this study was to identify consistent changes in measurands with hormone therapy and determine which reference interval is appropriate. METHODS: Laboratory data were abstracted from the medical records of 55 male-to-female patients on hormone therapy and compared with 20 male and 20 female nontransgender subjects. RESULTS: Hemoglobin, hematocrit, and low-density lipoprotein resembled female values (P < .005), while alkaline phosphatase, potassium, and creatinine resembled male values (P < .05). Triglycerides were higher (P < .005) than either the male or female groups. The remainder of the measurands showed no differences. CONCLUSIONS: Use of correct reference intervals in interpreting laboratory results reduces the risk of testing-related diagnostic error. Preliminary data suggest that new reference intervals need to be established for transgender patients.


Subject(s)
Biomarkers/blood , Gonadal Steroid Hormones/administration & dosage , Transgender Persons , Adult , Aged , Alkaline Phosphatase/blood , Cholesterol, LDL/blood , Creatinine/blood , Diagnostic Errors , Female , Hematocrit , Hemoglobins/metabolism , Humans , Male , Middle Aged , Potassium/blood , Reference Values , Sex Reassignment Procedures , Triglycerides/blood
7.
Kidney Int ; 74(2): 143-5, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18591943

ABSTRACT

Muscle wasting is a hallmark of uremic cachexia and has frequently been attributed to malnutrition that manifests as anorexia in chronic kidney disease. However, recent evidence indicates that proteolytic mechanisms are responsible for atrophy. Cheung and colleagues have reexamined the links between loss of lean body mass and nutrition. They demonstrate that neuropeptide signaling pathways, which regulate appetite and energy expenditure, also affect expression of key proteins involved in muscle mass maintenance.


Subject(s)
Cachexia/metabolism , Melanocortins/metabolism , Muscular Atrophy/metabolism , Uremia/complications , Animals , Appetite Regulation , Cachexia/etiology , Cachexia/prevention & control , Chronic Disease , Humans , Leptin/metabolism , Male , Melanocortins/antagonists & inhibitors , Mice , Muscle, Skeletal/metabolism , Muscular Atrophy/etiology , Muscular Atrophy/prevention & control , Nutritional Requirements , Signal Transduction
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