Theresa Lu holds the St. Giles Chair for Research in the HSS Research Institute, is a faculty member in Pediatric Rheumatology and in Rheumatology at HSS, and is Professor of Microbiology and Immunology and Professor Pediatrics at Weill Cornell Medicine. She is also currently Co-Director of the Weill Cornell PhD Program in Immunology and Microbial Pathogenesis. Dr. Lu received her MD and PhD from Yale University, trained in Pediatrics at Children's Hospital of Philadelphia, and completed her fellowship in Pediatric Rheumatology at the University of California San Francisco. She completed her PhD training with Joseph Madri at Yale and her postdoc training with Jason Cyster at UCSF. She has received numerous awards, including the American College of Rheumatology Young Investigator Award, Weill Cornell Teaching and Mentoring Award, and induction into the American Society for Clinical Investigation and the Henry Kunkel Society for immune disease research. Dr. Lu's goal is to better understand and treat lupus and other rheumatic diseases while also supporting the growth and development of the next generation of scientists.
The immune circuit in disease
The Lu Lab studies how the immune system interacts with tissues to limit or promote autoimmune and musculoskeletal diseases. There is a circuitry whereupon injury or infection, the affected tissue sends signals to lymphoid tissues such as lymph nodes, which are the sites of T and B cell activation. T and B cells in lymph nodes may become activated by these signals causing lymph node swelling, and then migrate from the lymph nodes to the affected tissue. There, they may help to control the infection but are also capable of inadvertently causing tissue destruction. In autoimmune and inflammatory diseases such as lupus, tissues such as the skin are more prone to injury to begin with, and there is activation of T and B cells that destroy tissues. We want to better understand the functions of the component parts of this circuitry as well as how the component parts interact to yield health versus disease. For example, we are asking 1) why tissues in disease are more prone to injury and 2) how signals from affected tissues modulate the lymph node microenvironment to regulate the activity of T and B cells.
We address the questions from a number of perspectives, including 1) lymph node vascular-stromal microenvironment that controls T and B cells in autoimmune and musculoskeletal conditions, 2) Langerhans (immune) cell protection of the skin in lupus photosensitivity ( a skin sensitivity to sunlight), 3) lymphatic dysfunction in disease, and 4) the role of immune cells in tissue repair and regeneration in fibrosis.
Our work has the potential to provide more insight into fundamental mechanisms of health and disease and to lead to better treatment of rheumatic and orthopedic conditions.
If you are interested in joining the Lu Lab, please send cover letter, CV, and contacts for 3 references to lut@hss.edu.
Please visit the Theresa Lu Lab page to see our publications and learn more about our lab and our work.
Lupus
Photosensitivity of skin
Lymphatics
Lymph node stromal cells
Fibroblastic reticular cells
Vasculature
Immune cell-tissue interactions
NIH R01 AI079178
DOD W81XWH-22-1-0627
NIH 1R21AR081493
St. Giles Foundation
A Lasting Mark Foundation
Barbara Volcker Center for Women and Rheumatic Diseases
Autoimmunity and Inflammation Program, HSS Research Institute
Division of Pediatric Rheumatology, Department of Medicine, HSS
Department of Microbiology and Immunology, Weill Cornell Medical School
Department of Pediatrics, Weill Cornell Medical School
Immunology and Microbial Pathogenesis Graduate Program, Weill Cornell Graduate School
St. Giles Chair for Research and Senior Scientist, HSS Research Institute
Faculty, Division of Pediatric Rheumatology, Department of Medicine, HSS
Professor of Microbiology and Immunology, Department of Microbiology and Immunology, Weill Cornell Medical School
Professor of Pediatrics, Department of Microbiology and Immunology, Weill Cornell Medical School
Co-director, Immunology and Microbial Pathogenesis Graduate Program, Weill Cornell Graduate School
BS Yale University
MD, PhD Yale University: PhD in the lab of Joseph Madri, PhD,MD
Pediatrics, Children's Hospital of Philadelphia
Pediatric Rheumatology, University of California, San Francisco
Postdoc in the lab of Jason Cyster, PhD
Pediatric Rheumatology
Weill Cornell Graduate School 2010 Dean's Award for Excellence in Teaching and Mentoring 2010
Induction into the American Society for Clinical Investigation 2011
Henry Kunkel Young Investigator Award, American College of Rheumatology 2011
Induction into the Henry Kunkel Society for immune-disease research 2015
St. Giles Chair for Pediatric Research 2020
English
For all publications, please see the PubMed listing.
One of the goals of HSS is to advance the science of orthopedic surgery, rheumatology, and related disciplines for the benefit of patients. Research staff at HSS may collaborate with outside companies for education, research and medical advances. HSS supports this collaboration in order to foster medical breakthroughs; however, HSS also believes that these collaborations must be disclosed.
As part of the disclosure process, this website lists Research staff collaborations with outside companies if the Research staff member received any payment during the prior year or expects to receive any payment in the next year. The disclosures are based on information provided by the Research staff and other sources and are updated regularly. Current ownership interests and leadership positions are also listed. Further information may be available on individual company websites.
As of April 27, 2020, Dr. Lu reported no relationships with healthcare industry.
By disclosing the collaborations of HSS Research staff with industry on this website, HSS and its Research staff make this information available to patients and the public, thus creating a transparent environment for those who are interested in this information. Further, the HSS Conflicts of Interest Policy does not permit payment of royalties on products developed by him/her that are used on patients at HSS.
The Hospital for Special Surgery (HSS) is proud to announce that this Summer’s cohort of undergraduate students have successfully completed the inaugural session of a biomedical research program in collaboration with the Macaulay Honors College (CUNY). This summer program provides undergraduate students with an immersive experience in biomedical research and access to the laboratories of HSS Research Institute and clinical research spaces throughout the HSS main campus.
By partnering program scholars with HSS’s world-class researchers as mentors, students are able to experience biomedical research and understand that this is also a career option for them. “While many students beginning college are understandably excited about becoming a doctor and helping patients, fewer understand that you can also make a difference through a career in biomedical research,” said Dr. Theresa Lu, scientific director of the HSS Macaulay Scholars Program. “It’s our privilege to open the doors of discovery to these exceptional students and we hope to ignite a lifelong commitment to advancing musculoskeletal health and biomedical science.”
HSS's unparalleled expertise in the field of musculoskeletal health provide students the opportunity to explore the intersection of medicine and science in a cutting edge environment, and scholars could witness firsthand how research drives advancements across a spectrum of medicine.
The selected students, from the prestigious Macaulay Honors College, were each paired with an established investigator and their group members to serve as their research mentors. Additionally, each student was provided with a stipend to support them throughout this eight-week program. The organizing committee was comprised of Dr. Lu along with HSS CSO Dr. Lionel Ivashkiv, Vice President of Research Rosemarie Gagliardi, Director of Research Institute Operations Nicole Seate-Martin, faculty member Dr. Alexis Sideris, Tri-Institutional MD-PhD student Stephanie Azzopardi, and Weill Cornell medical student Branden Sosa. Dr. Sideris and Stephanie Azzopardi are former Macaulay Honors College students themselves, and Branden Sosa graduated from CUNY’s Hunter College.
HSS remains committed to fostering lasting connections with these gifted scholars and they look forward to witnessing their development as scientists. The next Macaulay Scholars Program is slated to begin this upcoming academic year. Prospective scholars are encouraged to apply.
A research team led by Hospital for Special Surgery (HSS) Research Institute, in collaboration with Weill Cornell Medicine, has been awarded two grants, one from the Department of Defense and one from the National Institutes of Health (NIH), to conduct groundbreaking research regarding lupus flares. Sun exposure can trigger skin lesions and worsening of kidneys or other internal organs affected by lupus, but how inflammation at the skin leads to internal organ effects is unknown. The hope is that this study will identify the molecular pathways that drive photosensitivity and lupus flares to determine better treatment options for this confounding and mysterious disease.
The Department of Defense has granted a three-year grant to study the proteins emitted from the skin that affect lymph nodes, the downstream immune tissues, while a two-year grant from the NIH will aid the investigation into non-protein molecules and changes of fibroblasts in lymph nodes. The team will do this by examining skin components including interstitial fluid.
“My lab is focused on understanding the pathogenesis of lupus. Lupus skin rashes affect the quality of life of patients and can be connected to systemic disease that can be life-threatening. Therapeutic options in lupus are limited, and it is important that we understand pathologic mechanisms so that we can develop better therapeutic options,” said lead investigator Theresa T. Lu, MD, PhD, from HSS Research Institute.
The grants and research will be executed at HSS Research Institute, the largest musculoskeletal research facility in the world.
About HSS Research Institute
HSS Research Institute is the largest musculoskeletal research facility in the world. With over 300 dedicated researchers and 20 laboratories, HSS Research Institute has been a leader in research aimed at improving the lives of patients suffering from debilitating orthopedic and rheumatic conditions such as arthritis, bone and soft tissue injuries, autoimmune diseases, and musculoskeletal pain and deformities.
After sun exposure, people with systemic lupus erythematosus (SLE) frequently develop skin rashes, which often are accompanied by a flare of their overall disease. This connection between ultraviolet (UV) light and disease flares in lupus is well known, but the way in which UV exposure actually triggers the disease has been poorly understood.
In a new study being presented at ACR Convergence 2022, the annual meeting of the American College of Rheumatology, researchers from Hospital for Special Surgery (HSS) report that they have found an underlying mechanism that explains this association: decreased lymphatic drainage, which contributes to both photosensitivity and an immune response in the lymph nodes. The research also suggests that boosting lymphatic drainage may be an effective treatment for lupus photosensitivity and autoimmunity.
“When people with lupus have a systemic flare of their disease, it can affect any organ that is part of their disease,” says senior author Theresa T. Lu, MD, PhD, who holds the St. Giles Chair for Research in the HSS Research Institute, is a faculty member in Pediatric Rheumatology and in Rheumatology at HSS and is a professor of microbiology and immunology and of pediatrics at Weill Cornell Medicine. “We wanted to look at why sun exposure at the level of the skin affects internal organs like the kidneys, heart and lungs.”
“This study sheds some light on how sun exposure and UV light cause people with lupus to have more autoantibodies in their blood,” adds first author William Ambler, MD, a former fellow at HSS in Dr. Lu’s lab who is now Metzger Scholar in Translational Medicine at the National Institute of Arthritis and Musculoskeletal and Skin Diseases at the National Institutes of Health.
The skin communicates with the immune system by sending cells and molecular signals via the lymphatic vessels to the lymph nodes, where immune responses begin. The signals that the skin sends to the lymph nodes control the type of immune responses that occur. Lymphatic vessels also serve the function of removing fluid and cells from the skin. If lymphatic vessels do not work properly to bring signals from skin to lymph nodes, there can be delayed resolution of skin inflammation, leading to faulty signals being sent to the lymph nodes.
Research in the Lu lab suggests that lymphatic flow from the skin to the draining lymph nodes is reduced in people with lupus. The investigators hypothesize that this decreased flow alters lymph node immune responses, making them more pathogenic. They decided to look more closely at this communication and how it impacts immune function. The current research employed both patient samples and mouse models of SLE.
The investigators studied skin biopsies from lupus patients as well as from healthy volunteers who served as controls. When they looked at the samples from the lupus patients, they found these more dilated lymphatic vessels compared with the healthy controls. This provided evidence that people with lupus have poor lymphatic flow.
They then studied mouse models of SLE, using a dye injected into the skin to visualize the flow of lymphatic fluid. They found that when lupus mice were exposed to UV radiation, more dye remained in the skin. This provided evidence that the lymphatics were not clearing the fluid as well as they should.
Importantly, the researchers then looked to see if they could improve certain hallmarks of disease in the mice by using manual lymphatic drainage techniques to manipulate the flow of lymph fluid. This type of therapy is used in people with certain types of cancer, especially breast cancer, to prevent lymphedema (fluid accumulation and swelling) after the surgical removal of lymph nodes. They found that performing lymphatic drainage in the mice reduced the numbers of plasmablasts and germinal center B cells, types of cells that are known to be important players in lupus.
Drs. Ambler and Lu are optimistic that manual lymphatic drainage may benefit lupus patients but emphasize that clinical trials in patients are needed to confirm it would be safe and effective.
The investigators note that this research is also important because it advances the broader field of understanding how skin and organs communicate through the lymph nodes and the immune system.
Thanks to the generous support of donors, Hospital for Special Surgery (HSS) has announced the funding of nine grants for projects related to the study of COVID-19. These projects reflect the institution’s expertise in basic, translational and clinical research, and clinical care. Over $500,000 has been awarded so far.
HSS is the world’s largest academic medical center specialized in musculoskeletal health, spanning orthopedics, rheumatology and related disciplines. The HSS Research Institute maintains 20 laboratories dedicated to solving debilitating orthopedic and rheumatic conditions such as arthritis, bone and soft tissue injuries, autoimmune diseases, and musculoskeletal pain and deformities. There, more than 300 dedicated personnel focus on tissue repair, improving surgical outcomes, autoimmunity and inflammation, genomics, new treatments, and precision medicine.
“HSS has a long history of contributing to the collective base of clinical and basic science knowledge and finding healthcare solutions for complex conditions,” said Louis A. Shapiro, President and CEO, HSS. “We’re proud that through the joint efforts of our institution and philanthropic support, we will have the ability to make a strong impact on this growing and vital area of research.”
“As experts in inflammatory disorders and in the development of interventions for overactive immune responses, the clinicians and researchers at HSS are well-positioned to investigate many of the adverse effects of COVID-19,” says Lionel B. Ivashkiv, MD, Chief Scientific Officer at the HSS Research Institute. “This includes studying the causes of these adverse effects as well as how to prevent and treat them.”What follows are descriptions of the first group of funded projects in basic/translational research:
Activation of pDCs by SARS-CoV-2 and Its Impact on Macrophage Response
Principal Investigator: Franck Barrat, PhD
Co-Investigator: Marie-Dominique Ah Kioon, PhD
This project will study cell types that are responsible for cytokine storm syndrome — the hyperactive immune response seen in people with COVID-19 — by looking at how certain immune cells are activated by SARS-CoV-2. Research in mice infected with SARS-CoV, a coronavirus similar to the one that causes COVID-19, has suggested that plasmacytoid dendritic cell precursors (pDCs) are key to the immune response to infection. These pDCs activate macrophages, which in turn secrete cytokines. In the SARS-CoV research, depletion of pDCs appeared to protect the mice from lethal lung injury. Using blood samples from donors, the investigators will study the pathway by which pDCs activate macrophages and look at ways to therapeutically block that process.
Inhibiting RNA Polymerase II Transcription Complexes in Macrophages to Target COVID-19–Associated Cytokine Storm
Principal Investigator: Inez Rogatsky, PhD
Co-Investigators: Steven Josefowicz, PhD, and Robert P. Fisher, MD, PhD
This pilot project will dissect the role of macrophages in SARS-CoV-2-induced acute respiratory distress syndrome (ARDS), the main driver of COVID-19-associated mortality. We will test small-molecule inhibitors of RNA Polymerase II (Pol II) transcription complexes for their ability to modulate type I interferon and inflammatory pathways in monocytes/macrophages. This research will be done using cultured macrophages as well as donor blood and blood from COVID-19 patients.
Mechanisms of Cytokine Storm in Patients with COVID-19
Principal Investigator: Mary K. Crow, MD
Co-Investigators: Mikhail Olferiev, MD, and Lionel B. Ivashkiv, MD
The objectives of this study are to describe the process of the cytokine storm in people with COVID-19 and to identify biologic predictors of a favorable outcome in patients with severe cases of the disease. The project aims to characterize immune cell populations seen in COVID-19 patients who experience cytokine storm and compare them to those patients who do not, to compare the immune response before and after patients are given the anti-inflammatory drug anakinra, and to identify measures that suggest patients are more likely to decline and eventually require mechanical ventilation. The research will employ blood samples from HSS patients who are being treated for COVID-19 at New York–Presbyterian Hospital and who meet certain other qualifications.
What follows are descriptions of the first group of funded projects in the areas of clinical and health outcomes research:
Response to and Recovery from TKA in Patients with Antibodies to SARS-CoV-2
Principal Investigator: Miguel Otero, PhD
Co-Investigators: Meghan Kirksey, MD, PhD, and Peter K. Sculco, MD
It is unknown if people who have been exposed to COVID-19 may be at higher risk of experiencing an abnormal immune response following surgery, resulting in poor outcomes. This study will evaluate the response to and recovery from total knee arthroplasty (TKA) in people who have antibodies to COVID-19 — a marker of exposure. This study will include both patients who have COVID-19 antibodies and those who don’t, to act as controls. Patients will be followed for six weeks after surgery and evaluated for the presence of certain immune markers in the blood, as well as symptoms of inflammation including pain and stiffness in the joint.
SARS-CoV-2 Exposure and the Role of Vitamin D Among Hospital Employees
Principal Investigator: Emily M. Stein, MD, MS
Co-Investigators: Theresa T. Lu, MD, PhD; Andy O. Miller, MD; Jeri Nieves, PhD; and Alana Serota, MD
It is unknown if people with vitamin D deficiency may be more likely to become infected with COVID-19. This study will investigate vitamin D status and associated immune markers as risk factors for COVID-19 infection in a cohort of healthcare workers. Healthcare workers are at higher risk of contracting COVID-19 than the general population, making them a good group to study. Vitamin D is critical for immune function and is known to be protective against respiratory-tract infection and tuberculosis. This prospective, observational study will follow healthcare workers at HSS and at other healthcare facilities for one year, to determine whether levels of vitamin D and certain immune cells in the blood make someone more susceptible to COVID-19 infection.
Association of Immunomodulatory Medication Use and Social Determinants of Health with COVID-19 Infection in Systemic Rheumatic Disease Patients in New York City
Principal Investigator: Medha Barbhaiya, MD, MPH
Co-Investigators from HSS: Lisa Mandl, MD, MPH; Catherine MacLean, MD, PhD; Vinicius Antao, MD, PhD; Jane Salmon, MD; and Mayu Sasaki, MPH
Other Co-Investigators: Candace Feldman, MD, MPH (of Brigham and Women’s Hospital); Debra D’Angelo, MS (of Weill Cornell Medicine)
Using data from the INSIGHT Clinical Research Network, a central repository containing longitudinal electronic health data for residents of New York City, investigators will assemble a cohort of patients being treated with immunomodulatory medications for rheumatic disease. This patient population will then be used to study the effect of these medications on COVID-19 incidence and outcomes. Retrospective data will be used to evaluate the incidence and severity of COVID-19 in these patients. Patients will also be studied prospectively to determine whether there’s a relationship between COVID-19 infection and future rheumatic disease as well as to study connections between infection and future psycho-social issues.
Assessment of Surgical Outcomes in the COVID-19 Pandemic Era
Principal Investigator: Andy O. Miller, MD
Co-Investigators: Scott A. Rodeo, MD, and Mark Fontana, PhD
Investigators will implement a patient registry to evaluate how COVID-19 affects outcomes and complication rates after orthopedic surgery. This registry, along with COVID-19 screening procedures, will provide the tools to address specific research questions. Among these questions are determining the incidence of current and prior infection among the HSS surgical population, the clinical features associated with current and prior infections in this patient population, and whether COVID-19 status affects short-term complication rates.
What follows is a description of an integrated multidisciplinary study being undertaken jointly by the Adult Reconstruction and Joint Replacement (ARJR) Perioperative Research Group, Anesthesiology and Rheumatology:
Prediction and Prevention of Postoperative Blood Clots in COVID-19 Patients
Principal Investigators: Friedrich Boettner, MD; Kethy M. Jules-Elysee, MD; Lisa A. Mandl, MD, MPH
Co-Investigators: ARJR surgeons: Alejandro Gonzalez Della Valle, MD; Jason Blevins, MD; David J. Mayman, MD; Peter K. Sculco, MD; Geoffrey H. Westrich, MD and Thomas P. Sculco, MD
Medicine/Rheumatology: Medha Barbhaiya, MD, MPH; Doruk Erkan, MD, MPH; Deanna Jannat-Khah, DrPH
Pathology: Thomas W. Bauer, MD, PhD
Anesthesiology: Stavros G. Memtsoudis, MD, PhD, MBA; Alexandra Sideris, PhD
ARJR: Amethia Joseph, MHA; Ethan Krell, MS
Weill Cornell Medicine: Raymond David Pastore, MD
Recent literature suggests that one of the major complications seen in people with COVID-19 is thrombosis (the formation of blood clots) due to endothelial dysfunction, persistent inflammation and potentially antiphospholipid antibodies. As elective surgeries resume, those with prior exposure to SARS-CoV-2 will inevitably present for treatment, and some may have perioperative management considerations related to their risk of deep-vein thrombosis. This project will use, a noninvasive device that can determine clotting risks, to investigate whether people who have had COVID-19 have a more dysfunctional endothelium preoperatively and at 24 hours after surgery. The investigators will measure antiphospholipid antibodies and inflammatory markers, and evaluate the prevalence of asymptomatic post-operative deep-vein thrombosis in people who undergo TKR and have SARS-CoV-2 antibodies.
COVID-19 Translational Research Core at HSS
Principal Investigator: Theresa Lu, MD, PhD
Co-Investigators: Jessica Andrés-Bergós, PhD; Miguel Otero, PhD and Emily M. Stein, MD, MS
The COVID-19 Translational Research Core (TRC) was designed to fill critical gaps in the resources needed to promote the broad range of COVID-19–related clinical and translational research at HSS. The TRC will provide consultation on the design and implementation of COVID-19 research in the areas of orthopedics, rheumatology and metabolic bone disease; support for a COVID-19 biobank; and technical expertise and facilities required for clinical and translational researchers working on COVID-19–related projects. The TRC staff will help to acquire, house, and track biospecimens from investigator-initiated COVID-19–related research studies.
Lupus News Today featuring Theresa Lu, MD, PhD
European Biotechnology featured a study by HSS scientist Theresa T. Lu, MD, PhD, who investigated the potential link between immune cells and photosensitivity in patients with lupus.
According to the article, Dr. Lu and her researchers found that a malfunction of Langerhans cells meant to protect the skin from UV damage, could be causing photosensitivity.
Additionally, findings indicated that skin samples from lupus patients also had decreased numbers of Langerhans cells.
Read the full article at European-biotechnology.com.
Additional Coverage:
Rheumatic diseases affect women two to four times more often than men. Studying the sex differences in autoimmune conditions has been the focus of the Barbara Volcker Center for Women and Rheumatic Diseases at Hospital for Special Surgery. In a feature article by The Rheumatologist, HSS rheumatologists recall the history and ongoing mission of the Center as it celebrates its 20th anniversary.
HSS rheumatologist Michael D. Lockshin, MD, and director of the Center, shared his conversations with patient Barbara Volcker, wife of former U.S. Federal Reserve Chairman Paul Volcker. According to the article, Mrs. Volcker met Dr. Lockshin in the 1970s to treat her rheumatoid arthritis.
"She was the type of patient that I really enjoyed taking care of because she challenged me on everything. She would say, 'But that answer doesn't make sense. Give me the information behind it. Convince me.' She drove me to question my own assumptions to respond to her," said Dr. Lockshin.
In the late 1990s, Mrs. Volcker's health worsened, and the Volckers offered to establish a center at HSS to honor her. Dr. Steven Paget, who was physician in chief at HSS, and Dr. Charles Christian, who was the emeritus physician in chief, invited Dr. Lockshin, then acting director of the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), to discuss the center's mission, and he was ultimately offered the job as director, a position he still holds.
The Center was established in 1997. Mrs. Volcker passed away the following year at the age of 68.
"Her questions are the core of the Center that bears her name," noted Dr. Lockshin.
The Center convened a conference on the biology of sex differences in autoimmune illness—the first of its kind—within a year of opening its doors, notes Dr. Lockshin. The topic later gained national attention for all human health when the Institute of Medicine (later renamed the National Academy of Medicine) convened a committee to address the same question and published a report in 2001, according to Dr. Lockshin, who served on the committee. Doruk Erkan, MD, MPH, a rheumatologist at HSS whose early research focused on antiphospholipid syndrome, joined the Center in 2005 as physician-scientist.
Today, the Center is marking 20 years of research and clinical work devoted to women with various rheumatic conditions. According to Dr. Lockshin, physicians at the Center see more than 3,000 individual patients for issues of pregnancy and contraception, antiphospholipid syndrome, and other rheumatic illnesses.
As part of the Center's research, HSS rheumatologists Jane E. Salmon, MD and Lisa R. Sammaritano, MD are co-investigators of a study on hormone treatment in lupus as well as pregnancy in lupus patients.
Additionally, HSS research associate Mikhail Olferiev, MD received a grant from the center to study the expression of genes across health donors and patients with lupus. "I hope that my study will contribute to a better understanding of an autoimmune disease and possibly identify new therapeutic targets," Dr. Olferiev said.
HSS scientist Theresa T. Lu, MD, PhD also received a grant to study whether fat tissue might influence stromal cells in lymph nodes to contribute to sex differences in rheumatic diseases.
Dr. Lockshin explained that concepts and ideas about pregnancy and issues related to women with rheumatic diseases have changed over time in part because of research discoveries coming out of HSS.
Additionally, the Center recently welcomed a new member, HSS rheumatologist Medha Barbhaiya, MD, MPH. Dr. Barbhaiya explained that she joined HSS because of the Center's strong emphasis on clinical care and clinical research related to lupus, antiphospholipid syndrome, and pregnancy in rheumatic diseases.
Several of its members hold leadership positions associated with the Center's mission, according to Dr. Lockshin. For example, Dr. Erkan chairs both the Antiphospholipid Syndrome Alliance for Clinical Trials and International Networking, headquartered at the Center, and the 15th International Congress on Antiphospholipid Antibodies. Kyriakos Kirou, MD, conducts lupus nephritis clinical trials, and Dr. Sammaritano chairs the ACR Reproductive Health Guideline Project. With a background in environmental causes of autoimmune illnesses, Dr. Barbhaiya is involved with the ACR. In addition, Dr. Lockshin served on committees with a focus on pregnancy, sex differences, and other aspects of autoimmune illness and he is past editor in chief of Arthritis & Rheumatism (now Arthritis & Rheumatology).
In a phone interview, Mr. Volcker said that he is delighted with the Center's accomplishments over the years. Furthermore, he said he is sure if Mrs. Volcker were alive she would be "very pleased and happy that her name was attached to it, no doubt in my mind".
Read the full article at the-rheumatologist.org. This also appeared in the January 2018 print issue.