Mikel Gurrea-Rubio

Division of Rheumatology, Department of Internal Medicine, and Clinical Autoimmunity Center of Excellence, University of Michigan, Ann Arbor, Michigan, USA.

14 publications 2021 – 2025 ORCID

What does Mikel Gurrea-Rubio research?

Mikel Gurrea-Rubio studies the role of specific proteins in causing inflammatory arthritis, which is a painful condition that results from the immune system attacking the joints. One of the main proteins he examines is called CD13, which leaks into the bloodstream and activates a receptor known as B1R on immune cells. His research has shown that this activation is particularly strong in patients with rheumatoid arthritis, leading to increased inflammation. By understanding this process, he aims to find targeted treatments that can block this receptor, potentially offering relief to people suffering from rheumatoid arthritis and other similar inflammatory diseases.

Key findings

  • Blocking the B1R receptor effectively stopped inflammation in both human tissue samples and in mouse models of arthritis.
  • The CD13 protein was found to be leaking into the bloodstream, which plays a critical role in the activation of inflammatory responses.
  • The activation of the B1R receptor was shown to be overactive in patients with rheumatoid arthritis, highlighting a new potential drug target.

Frequently asked questions

Does Dr. Gurrea-Rubio study rheumatoid arthritis?
Yes, he specifically researches the mechanisms behind inflammatory arthritis, including rheumatoid arthritis.
What treatments has Dr. Gurrea-Rubio researched?
He has investigated blocking the B1R receptor to treat inflammation associated with rheumatoid arthritis.
Is Dr. Gurrea-Rubio's work relevant to patients with inflammatory diseases?
Yes, his research could lead to new treatment options for various inflammatory diseases, particularly rheumatoid arthritis.

Publications in plain English

Targeting CD13/Aminopeptidase N as a Novel Therapeutic Approach for Scleroderma Fibrosis.

2025

Arthritis & rheumatology (Hoboken, N.J.)

Muraoka S, Brodie WD, Mattichak MN, Gurrea-Rubio M, Ikari Y +22 more

Plain English
This study focused on a condition called systemic sclerosis (SSc), an autoimmune disease that leads to thickening and scarring of the skin. Researchers found that certain proteins (CD13 and B1 receptor) were more active in the skin of patients with a severe form of SSc, contributing to excessive scar formation. By blocking the B1 receptor, they were able to reduce the fibrosis-related responses in lab tests and in mice, showing that this approach could be a new way to treat SSc. Who this helps: This helps patients with systemic sclerosis and their doctors by potentially offering a new treatment option.

PubMed

CD6 in Human Disease.

2025

Cells

Gurrea-Rubio M, Fox DA, Castresana JS

Plain English
This study examined the role of a protein called CD6, which is found on certain immune cells. Researchers found that CD6 is linked to more than 15 diseases, particularly autoimmune conditions, and it may play a role in cancer treatment as a therapy target. Understanding CD6's functions could lead to better ways to treat these diseases, helping more patients manage their health effectively. Who this helps: Patients with autoimmune diseases and cancer.

PubMed

Soluble CD13 is a potential mediator of neutrophil-induced thrombogenic inflammation in SARS-CoV-2 infection.

2025

JCI insight

Tsou PS, Ali RA, Lu C, Sule G, Carmona-Rivera C +41 more

Plain English
This study looked at a substance called soluble CD13 (sCD13), which is produced during COVID-19 infections. Researchers found that patients with severe COVID-19 had much higher levels of sCD13, and this was linked to increased inflammation and complications. Specifically, elevated sCD13 levels were associated with heightened immune response processes that lead to blood vessel stress and clot formation. Who this helps: This research benefits COVID-19 patients and doctors by highlighting possible targets for new treatments.

PubMed

Siponimod Attenuates Neuronal Cell Death Triggered by Neuroinflammation via NFκB and Mitochondrial Pathways.

2024

International journal of molecular sciences

Gurrea-Rubio M, Wang Q, Mills EA, Wu Q, Pitt D +3 more

Plain English
This study examined how siponimod, a medication approved for treating a form of multiple sclerosis called secondary progressive MS (SPMS), protects brain cells from damage caused by inflammation. Researchers found that siponimod significantly reduced cell death triggered by the inflammatory substance TNF-alpha in both rat and human brain cells, suggesting it helps to keep brain cells alive during neuroinflammation. This matters because it could lead to better treatment options for progressive forms of MS, which currently have limited effective therapies. Who this helps: This helps patients with secondary progressive multiple sclerosis.

PubMed

Ligands of CD6: roles in the pathogenesis and treatment of cancer.

2024

Frontiers in immunology

Gurrea-Rubio M, Lin F, Wicha MS, Mao-Draayer Y, Fox DA

Plain English
This paper studied the role of a protein called CD6 in T cells and how it interacts with other proteins in cancer. Researchers found that CD6 binds to three different proteins (CD166, CD318, and CD44) that are often present in cancer cells and are linked to worse outcomes for patients. Understanding these interactions could help improve cancer treatments and lead to better outcomes for patients. Who this helps: This benefits cancer patients and doctors working in oncology.

PubMed

Activation of cytotoxic lymphocytes through CD6 enhances killing of cancer cells.

2024

Cancer immunology, immunotherapy : CII

Gurrea-Rubio M, Wu Q, Amin MA, Tsou PS, Campbell PL +14 more

Plain English
This study investigated how a special antibody, UMCD6, affects immune cells that fight cancer. Researchers found that UMCD6 helps these immune cells, particularly natural killer (NK) cells and certain T cells, become more effective at killing cancer cells in mice with breast and prostate cancer, leading to improved survival rates. Specifically, treated mice had more powerful immune cells that were better positioned to attack tumors compared to those treated with a standard antibody. Who this helps: This benefits cancer patients by potentially improving treatments that enhance their immune responses to tumors.

PubMed

Activation of Cytotoxic Lymphocytes Through CD6 Enhances Killing of Cancer Cells.

2023

Research square

Gurrea-Rubio M, Wu Q, Amin MA, Tsou PS, Campbell PL +14 more

Plain English
This study looked at a specific way to boost the immune system's ability to fight cancer by focusing on a molecule called CD6. Researchers found that using an antibody (UMCD6) to block the interaction between CD6 and a protein found on many cancer cells (CD318) led to better survival rates in mice with breast and prostate cancer. In these mice, more immune cells that attack tumors, like NK and CD8+ T cells, were present and more active compared to those that didn’t receive the treatment. Who this helps: This benefits cancer patients by potentially improving treatment outcomes.

PubMed

Functional Characterization of Glycoprotein Nonmetastatic Melanoma Protein B in Scleroderma Fibrosis.

2022

Frontiers in immunology

Palisoc PJ, Vaikutis L, Gurrea-Rubio M, Model EN, O'mara MM +5 more

Plain English
This study looked at how a protein called GPNMB behaves in the skin cells of patients with diffuse cutaneous scleroderma (dcSSc), a condition that causes skin thickening. Researchers found that the levels of GPNMB were higher in skin cells from dcSSc patients compared to healthy individuals, with notable levels of its soluble form measured at 147.4 pg/ml versus 84.8 pg/ml. This protein appears to help reduce cell activity that leads to fibrosis, suggesting that boosting GPNMB could be a new way to treat scleroderma. Who this helps: This benefits patients with scleroderma.

PubMed

Inhibition of bromodomain extraterminal histone readers alleviates skin fibrosis in experimental models of scleroderma.

2022

JCI insight

Vichaikul S, Gurrea-Rubio M, Amin MA, Campbell PL, Wu Q +14 more

Plain English
This study looked at how blocking certain proteins called bromodomain extraterminal (BET) proteins can help reduce skin thickening in a condition known as scleroderma. The researchers found that using a drug called JQ1 to inhibit these proteins led to a significant reduction in fibrosis in lab animals and skin cells from scleroderma patients. Specifically, they observed changes in gene activity that affect cell growth and calcium levels, which are important for managing tissue fibrosis. Who this helps: This benefits patients with scleroderma by offering potential new treatment options.

PubMed

The dual role of CD6 as a therapeutic target in cancer and autoimmune disease.

2022

Frontiers in medicine

Gurrea-Rubio M, Fox DA

Plain English
This study looks at how CD6, a molecule in the immune system, plays a role in both cancer and autoimmune diseases. Researchers found that CD6 can be a potential target for treatments since it affects how the immune system reacts to both cancer cells and self-antigens, the body's own proteins that can trigger autoimmune responses. This is important because finding ways to effectively manage cancer treatment while minimizing autoimmune issues could greatly improve patient outcomes. Who this helps: This helps patients with cancer and autoimmune diseases, as well as their doctors.

PubMed

Soluble CD13 induces inflammatory arthritis by activating the bradykinin receptor B1.

2022

The Journal of clinical investigation

Tsou PS, Lu C, Gurrea-Rubio M, Muraoka S, Campbell PL +26 more

Plain English
Researchers discovered that a protein called CD13, which leaks into the bloodstream, causes inflammatory arthritis by activating a receptor called B1R found on joint cells. They confirmed this by showing that blocking B1R with drugs stopped the inflammation in multiple types of arthritis in mice and in human joint tissue samples. This matters because B1R could be a new drug target to treat rheumatoid arthritis and other inflammatory diseases by preventing CD13 from triggering joint inflammation.

PubMed

Lymphocyte subset abnormalities in early diffuse cutaneous systemic sclerosis.

2021

Arthritis research & therapy

Fox DA, Lundy SK, Whitfield ML, Berrocal V, Campbell P +10 more

Plain English
This study looked at immune system changes in patients with early diffuse cutaneous systemic sclerosis (SSc), a condition that hardens the skin. Researchers found that these patients had more CD4+ T cells but fewer CD8+ T cells than healthy individuals, with a significant increase in a specific type of T cell known as CD319+ cells. These findings are important because the CD319+ T cells may help us understand how the disease develops and could be targeted for new therapies. Who this helps: This helps patients with systemic sclerosis by identifying potential new treatment options.

PubMed

Correction to: Lymphocyte subset abnormalities in early diffuse cutaneous systemic sclerosis.

2021

Arthritis research & therapy

Fox DA, Lundy SK, Whitfield ML, Berrocal V, Campbell P +10 more

PubMed

CD6 is a target for cancer immunotherapy.

2021

JCI insight

Ruth JH, Gurrea-Rubio M, Athukorala KS, Rasmussen SM, Weber DP +13 more

Plain English
This research studied a new cancer treatment involving a specific antibody called UMCD6 that targets a protein known as CD6. The findings showed that UMCD6 significantly improved the ability of immune cells to kill breast, lung, and prostate cancer cells, leading to more effective cancer cell death than traditional treatments that block certain immune checkpoints. This is important because it not only enhances cancer killing but also helps control autoimmune responses, making it a promising new approach for cancer immunotherapy. Who this helps: This benefits cancer patients and doctors seeking more effective treatment options.

PubMed

Publication data sourced from PubMed . Plain-English summaries generated by AI. Not medical advice.