Can Lyme Disease Trigger Autoimmune Disease Like Lupus?
Lyme disease may trigger autoimmune disease in some patients, including conditions such as lupus. In rare cases, infection with Borrelia burgdorferi may contribute to immune dysregulation and the development of new autoimmune symptoms.
Can Lyme Disease Trigger Autoimmune Disease?
In their article “Lyme Borreliosis as a Trigger for Autoimmune Disease,” Yehudina and colleagues present a case in which an infection with Borrelia burgdorferi (the bacteria that causes Lyme disease) triggered systemic lupus erythematosus (SLE), commonly referred to as lupus.1
As the authors explain, “long-term exposure of the host’s immune system to [Borrelia] spirochetes can contribute to the development of [a new onset] chronic autoimmune disease.”
This case report describes a 35-year-old woman who developed joint pain in her hands, low-grade fevers, fatigue, and skin rashes on her hands and trunk. She reported an insect bite prior to the onset of symptoms.
Initially, she was treated by a dermatologist with topical steroids for presumed dermatitis, but her symptoms did not improve.
She was later evaluated by a rheumatologist, who ordered Lyme disease testing. Her results were positive by Western blot, and she was treated with a 28-day course of doxycycline.
“Following therapy, her general condition improved with resolution of joint pain, weakness, normalization of body temperature, and decrease in rashes,” the authors report.
Autoimmune Symptoms Following Lyme Disease Treatment
Two months after completing treatment, the patient developed new symptoms, including low-grade fevers, a butterfly-shaped facial rash, hair loss, joint pain, morning stiffness, weight loss, and pronounced cold sensitivity in the fingers.
Given the change in her clinical presentation, further testing was performed to evaluate for systemic autoimmune disease.
A skin biopsy confirmed a diagnosis of lupus.
After treatment for the autoimmune condition, her symptoms improved significantly.
Possible Link Between Lyme Disease and Autoimmune Disease
The authors conclude that prolonged immune system exposure to spirochetes may contribute to the development of autoimmune disease.
One possible explanation for persistent symptoms or autoimmune reactions following Lyme disease is molecular mimicry, where the immune system mistakenly targets the body’s own tissues after responding to infection.
To explore how Lyme disease can mimic or overlap with autoimmune conditions, see can Lyme disease trigger an autoimmune disease?.
Related Articles:
Can Lyme disease trigger an autoimmune disease?
Lyme disease mimics autoimmune disorder
Lyme disease manifests as autoimmune disorder, Sjogren’s syndrome
References:
- Yehudina Y, Trypilka S. Lyme Borreliosis as a Trigger for Autoimmune Disease. Cureus. 2021 Oct 10;13(10):e18648. doi: 10.7759/cureus.18648. PMID: 34786243; PMCID: PMC8578812.
Dr. Daniel Cameron, MD, MPH
Lyme disease clinician with over 30 years of experience and past president of ILADS.
Symptoms • Testing • Coinfections • Recovery • Pediatric • Prevention
Sjogrens, atypical—seronegative with neurological involvement/dysautonomia. Have a history of Lyme, Bartonella, Mycoplasma.
Hi I would find it super helpful to find out the actual “autoimmune Treatment” that was received. Thank you
At the time that I was diagnosed with a +ANA for Lupus with a presentation of pleurisy, the follow-up was using Meloxicam and Hydroxychloroquine between 2009-2015. As symptoms seemed to be well managed, the Meloxicam (15) was halved, then ultimately d/c, as was the Hydroxychloroquine.
Interesting information regarding Lyme/Lupus connection. If it is, in fact, a mimicry of lupus as opposed to diagnosed Lupus, I would love to understand the underlying biochemistry. (I have a history of Lyme and aggressive treatment with months of IV therapy 22 years ago and eight years later experienced what I thought was connected to Lyme but proved to be a positive ANA for Lupus, with pleurisy as the major symptom. I continued under a Rheumatologist care 2009-2015, using Meloxicam 7.5 and Hydroxychloroquine. However, after seeing a Rheumatologist in 2017, she did not concur with the Lupus diagnosis, in spite of a +ANA, as I do not present as having Lupus. I dc the drugs. I haven’t been under treatment since 2017. While the infection left some arthritic conditions in its wake, it is not possible for me to differentiate as to whether the arthritis is post Lyme or the aging process of a decade’s long athlete.
I have patients who have been dismissed as having post Lyme for years without being evaluated for a persistent tick borne infection who have benefits from retreatment.
Join the club. We seem to all suffer the same dilemma. What is it? What’s causing it? I’ve even read many stories about how people who had a periodontal treatment ended up with Lyme disease and other autoimmune disease a few weeks or months later. Testing alone is not reliable in my opinion but maybe better tests have evolved in recent years. I tested positive for Sjogren’s and my family has a history of it on my mother’s side. But I never had any symptoms so I didn’t pay it any concern. 8 years later, it suddenly hit me with full force and this year, Lupus. All through my Lyme treatment, I never had any arthritis or swollen joints. I only suffered neurological symptoms including trigeminal and glossopharyngeal neuralgia and bone pain.
Aging probably bears some blame given how our hormones change and I’ve read that as estrogen levels drop, our immune system changes.
I have patients with Lyme disease who had thought they were suffering from Sjogren’s
The first time I posted on here was in regard to an article you posted about Sjogren’s and Lyme. I believe that Lyme or other tickborn pathogens trigger these autoimmune diseases. I also believe that Herpes viruses also do the same by “confusing” our immune system after prolonged infection.
I wish your office was closer. I thought you were in TX but you’re in NY. That’s too far for me to travel. Even Northern VA Internal Medicine ( Dr. Shor) is a bit far for me to travel on a regular basis when I feel this bad.
I am sorry to hear
Dr. Cameron, I’ve written on this site before but I won’t repeat all the details. After Lyme in 2016, I developed Sjogren’s in 2024 and now Lupus in ’25. I feel absolutely horrible all over and in immense pain in my knees and elbows. This is the most frustrating experience and I am determined to help myself without visiting a doctor. I know that may sound ignorant and irresponsible, but medical care in the US is so exhausting, impersonal and ineffective. I know I would feel even worse from all the stress and frustration.
Just wanted to share my most recent symptoms in regard to the article.
Female, 64 yrs. , VA
I am sorry you are still sick. It sounds like avoiding doctors is not working all that well either
Yes, yes. I hear you. Lesser of evils I suppose. There is a wonderful doctor here who has a Functional medicine practice and I’m considering a visit with her. I’ve heard wonderful things about her from other patients who have autoimmune disorders.
I feel better when looking at your dogs’ thumbnail picture. Perhaps I’ll rescue a dog. Dog’s are always the best medicine in my opinion 😀
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