International Journal of Trichology

: 2018  |  Volume : 10  |  Issue : 6  |  Page : 286--288

Suspected herpes zoster-associated encephalitis during treatment with oral tofacitinib in alopecia universalis

Anna-Marie Hosking, Margit Juhász, Natasha Atanaskova Mesinkovska 
 Department of Dermatology, University of California, Irvine, California, USA

Correspondence Address:
Ms. Anna-Marie Hosking
Department of Dermatology, University of California, 118 Med Surge I, Irvine 92697, California


Systemic administration of Janus kinase inhibitors (JAKis) is associated with adverse events, including serious infections, malignancy, and herpes zoster (HZ). Herein, we report a case of a 17-year-old male with alopecia universalis who developed suspected HZ-associated encephalitis (HZAE) during treatment with oral tofacitinib. Oral tofacitinib was immediately discontinued, and the patient was started on antiviral treatment. We present this case to highlight a serious complication that can arise with oral JAKi therapy. Physicians should have a high index of clinical suspicion for HZAE in any patient presenting with a vesicular rash and concomitant neurologic impairments while systemically immunosuppressed.

How to cite this article:
Hosking AM, Juhász M, Mesinkovska NA. Suspected herpes zoster-associated encephalitis during treatment with oral tofacitinib in alopecia universalis.Int J Trichol 2018;10:286-288

How to cite this URL:
Hosking AM, Juhász M, Mesinkovska NA. Suspected herpes zoster-associated encephalitis during treatment with oral tofacitinib in alopecia universalis. Int J Trichol [serial online] 2018 [cited 2023 Jan 28 ];10:286-288
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Full Text


Tofacitinib, a small-molecule Janus kinase (JAK) inhibitor (JAKi), was first approved for the treatment of rheumatoid arthritis in 2012 and later psoriatic arthritis in 2017. Tofacitinib is a JAK1/JAK3 inhibitor that attenuates the immune response, specifically T-cell-mediated inflammation through the downregulation of several inflammatory cytokines.[1] Tofacitinib has been used off-label to treat of alopecia areata (AA), with systemic formulations demonstrating promising results.[2]

JAKi are associated with an increased risk of infection. In particular, tofacitinib has been associated with serious infections in 2%–6% of patients, malignancy in 1%–3%, and herpes zoster (HZ) in 1%–3%.[3] Reactivation of varicella-zoster virus (VZV), known clinically as HZ or shingles, is associated with decreased VZV-specific cell-mediated immunity seen with advanced age (8-fold to 10-fold increased incidence in patients over 60 years) or immunosuppression (i.e., HIV/AIDS, bone marrow transplant, and iatrogenic systemic immunosuppression).[4] After primary infection, VZV remains latent in ganglionic neurons; upon reactivation, VZV travels anterograde to the skin, causing the hallmark dermatomal, vesicular rash. VZV can also travel retrograde, causing neurologic complications including encephalitis, meningitis, myelitis, optic neuritis, and stroke.[5]

 Case Report

A 17-year-old male with a 10-year history of AA progressing to alopecia universalis, with eyebrow and eyelash involvement, was started on oral tofacitinib 5 mg twice daily. The patient initially demonstrated successful therapeutic response with complete regrowth after JAKi initiation. Five months after starting tofacitinib, the patient presented to his family physician with painful, erythematous vesicles localized to the left chest wall in a dermatomal distribution associated with fever, malaise, new-onset severe headache, generalized weakness, mild cognitive impairment, confusion, somnolence, psychomotor agitation, and new-onset paresthesias of his hands and feet. The diagnosis of HZ with complications was made, and he received oral valacyclovir 1000 mg three times a day for 7 days with instructions to go to the emergency department if symptoms worsened; a spinal tap was not performed. Oral tofacitinib was immediately discontinued. After antiviral treatment, the patient's symptoms gradually improved to resolution without sequelae. Oral tofacitinib was restarted; however, the patient started to lose hair and continued despite increasing tofacitinib dose; after 2 months without clinical response, JAKi was discontinued [Figure 1].{Figure 1}


HZ is a known adverse event secondary to immunosuppression with oral JAKis. In particular, patients taking tofacitinib 10 mg twice daily (vs. 5 mg twice daily), those of Asian race (Japanese and Korean), older age, and those with prior biologic use are at increased risk.[6] Furthermore, increased risk of developing HZ is well documented in patients with autoimmune diseases, including AA, and is likely secondary to the use of systemic immunosuppressive medications. Although HZ is usually self-limited, in rare cases and in the setting of immunosuppression, disseminated HZ can occur leading to complications including encephalitis and even death.[7]

Clinical diagnosis of HZ-associated encephalitis (HZAE) is made based on the presence of the characteristic HZ rash and symptoms of encephalitis (including but not limited to fever, malaise, headache, and cognitive impairment) [Table 1].[8] Patients usually present with delirium days after the outbreak of a vesicular rash, but symptoms may occur before the rash, up to 6 months after, or even in the absence of the classic dermatomal rash (zoster sine herpete). Encephalitis due to VZV is characterized by concomitant vasculopathy affecting either large or small vessels. Large-vessel disease (granulomatous arteritis) is seen in immunocompetent hosts, whereas small-vessel disease is commonly found in the setting of immunodeficiency. Complications of HZAE include intracerebral hemorrhage and stroke.[5]{Table 1}

HZAE has been reported with the use of oral tofacitinib in another case. A 51-year-old Caucasian male in an ulcerative colitis clinical trial developed HZAE after taking tofacitinib 10 mg twice daily for over 2 years. Tofacitinib was permanently discontinued, and the patient was treated with intravenous acyclovir, followed by oral valacyclovir. Symptoms resolved and there were no reported sequelae.[9]

The patient discussed in this report matched diagnostic criteria for possible encephalitis: (1) The presence of altered mental status for more than 24 h with no alternative cause identified (major criterion), (2) documented fever, and (3) new-onset neurologic findings (two minor criteria). He did not present with seizures, and diagnostic tests such as spinal tap, electroencephalography, or brain imaging were not performed. Abnormalities in any of the aforementioned tests would have resulted in three or more positive minor criteria, which qualify as probable or confirmed encephalitis. As brain computed tomography (CT) imaging is often unremarkable in HZAE, the best diagnostic test is polymerase chain reaction identification of VZV in cerebrospinal fluid. First-line treatment of HZAE includes prompt discontinuation of systemic immunosuppression, if applicable, and intravenous acyclovir should be administered as early as possible to prevent long-term neurologic sequelae.


Oral JAKi therapy may be associated with HZ skin lesions accompanied by systemic neurologic symptoms, which can clinically present as encephalitis. Given the increasing use of systemic JAKi in dermatology, physicians should be acutely aware of the opportunistic infections associated with systemic immunosuppressive medications, as well as their complications. For patients taking oral JAKi who present with characteristic HZ vesicular lesions and associated central neurologic symptoms, clinicians should suspect HZAE.[10]

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given his consent for his images and other clinical information to be reported in the journal. The patient understands that his name and initials will not be published and due efforts will be made to conceal identity, but anonymity cannot be guaranteed.

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Conflicts of interest

There are no conflicts of interest.


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