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MMR + varicella zoster vaccine (MMRV zoster vaccine)

✓ Approved

GSK · 疫苗 · 疫苗

什么是 MMR + varicella zoster vaccine?

MMR + varicella zoster vaccine 是一种疫苗,由GSK研发。该药已获批,用于治疗相关适应症,给药途径:Injectable (Others)、Intramuscular (IM) Injection、Subcutaneous Injection。

药物档案

商品名MMRV zoster vaccine
公司GSK
药物类别疫苗, 大分子
给药途径Injectable (Others), Intramuscular (IM) Injection, Subcutaneous Injection
状态Approved

治疗适应症

MMR + varicella zoster vaccine 针对 3 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Infections and infestationsSalmonellosis✓ Approved
Infections and infestationsMeasles✓ Approved
Infections and infestationsVaricella zoster virus infection✓ Approved

相关研究文献

PubMedCureus2026-09-10

Recurrent Mumps in a Fully Vaccinated Young Adult With a Prior Breakthrough Infection: A Case Report.

Ramadugu Rithika R, Pidikiti Chandra Varshini CV, Cordero Peña Alesha A, Almonte Angelis A et al.

Mumps is a vaccine-preventable viral disease that typically presents with parotid gland swelling and constitutional symptoms. Although widespread immunization has substantially reduced disease incidence, outbreaks continue to occur among vaccinated populations, raising concerns regarding waning immunity and vaccine failure. Recurrent mumps following both prior natural infection and complete vaccination is uncommon and remains infrequently reported. We describe a 21-year-old woman who presented with a four-day history of fever, malaise, myalgia, and progressive painful swelling of the left parotid gland associated with difficulty chewing and speaking. She had received two doses of measles-mumps-rubella (MMR) vaccine according to the national immunization schedule and had a documented history of mumps infection at nine years of age, occurring after she had already completed her two-dose MMR series (vaccine-breakthrough infection). Physical examination revealed tender unilateral parotid enlargement, cervical lymphadenopathy, and evidence of undernutrition with a body mass index of 16.7 kg/m². Laboratory evaluation demonstrated iron deficiency anemia. Further evaluation, including positive mumps RT-PCR and positive anti-mumps IgM serology, confirmed acute mumps infection, while investigations excluded alternative causes of parotid enlargement. The patient was managed conservatively with isolation, supportive care, nutritional supplementation, and symptomatic treatment, resulting in complete clinical recovery without complications. This case highlights that recurrent mumps can occur despite prior natural infection and complete MMR vaccination. Although waning immunity and host factors such as undernutrition may have contributed to susceptibility, a causal relationship cannot be established from a single case. Continued surveillance and awareness of breakthrough infections remain important, particularly in resource-limited settings.

PMID 42719503
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PubMedClinical case reports2026-09-10

Dermatome-Specific Herpes Zoster Following Corticosteroid Therapy for Lumbar Disc Herniation: A Case Report Illustrating the Immunocompromised District Theory.

Liu Jun J, Luo Lili L, Zhou Ming M, Chen Weifeng W et al.

Systemic corticosteroids frequently utilized to manage lumbosacral radiculopathy introduce an immunological paradox by potentially triggering varicella-zoster virus reactivation. While well-documented in severely immunocompromised populations, the specific neuro-immunological mechanisms in otherwise immunocompetent patients with lumbar disc herniation remain underappreciated. This case presents an observation conceptually relevant to the "Immunocompromised District" theory, proposing a theoretical link between acute radicular compression and a localized vulnerability that may correlate with the precise anatomical distribution of a viral outbreak. A 52-year-old male presented with acute mechanical right-sided lumbar and anterior thigh pain. Magnetic resonance imaging revealed an acute L3-L4 disc herniation compressing the L4 nerve root, coexisting with an asymptomatic chronic L4-L5 herniation. Four days after initiating intravenous dexamethasone, the patient experienced a sudden phenotypic shift in symptoms: the mechanical dullness transformed into severe, electric-shock-like neuropathic pain. This heralded a herpes zoster eruption remarkably confined to the acutely symptomatic L4 dermatome, completely sparing the chronically compressed L5 region. Following corticosteroid discontinuation and initiation of antiviral therapy, the lesions resolved within 1 week, leaving mild post-herpetic neuralgia at the one-month follow-up. Given the lack of objective molecular data, we hypothesize a multifactorial pathogenesis for this phenomenon. A theoretical "double hit" mechanism-comprising corticosteroid-induced systemic immunosuppression and localized vulnerability from acute radiculopathy-may potentially facilitate viral reactivation in a susceptible host (e.g., possessing age-related and metabolic risk factors). Clinically, a sudden qualitative shift in pain phenotype from mechanical to neuropathic during steroid therapy for lumbar degeneration may serve as an early clinical clue of impending herpes zoster. Recognizing this dynamic prevents misinterpreting viral prodromes as mechanical exacerbations, thereby avoiding the detrimental escalation of immunosuppressive therapy.

PMID 42719596
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PubMedHuman mutation2026-09-10

Bayesian Integration of Tumor Mutational Signatures and Somatic Features Refines Pathogenicity Assessment of Germline Mismatch Repair Variants.

Amzaleg Yonatan Y, McDonnell Kevin J KJ, Idos Gregory E GE, Mathai Christina C et al.

Variants of uncertain significance (VUS) in mismatch repair (MMR) genes represent a persistent bottleneck in germline interpretation for Lynch syndrome, creating a critical opportunity to leverage tumor biology to refine pathogenicity assessment. Although tumor features such as microsatellite instability (MSI) and immunohistochemistry (IHC) are routinely evaluated, they are typically interpreted separately from germline classification, and their quantitative contribution within ACMG/AMP frameworks remains poorly defined. We therefore analyzed paired germline and tumor sequencing data from 1110 tumors across 1073 patients with colorectal or endometrial cancer to determine whether mismatch repair-deficient (MMR-d) mutational signatures can be quantitatively integrated into Bayesian germline variant interpretation. Using COSMIC single-base substitution signatures, tumors were classified as MMR-d or MMR proficient, and an empirically derived likelihood ratio (LR) quantified the association between MMR-d signatures and pathogenic germline MMR variants. The presence of an MMR-d signature increased the likelihood of an underlying pathogenic germline MMR variant approximately eightfold (LR ≈ 8; log10 LR ≈ 0.90), whereas its absence provided moderate-to-strong benign evidence (LR ≈ 0.156; log10 LR ≈ -0.81). Applying this integrative framework to 45 germline MMR VUS, joint modeling of tumor mutational signatures with additional somatic and variant-level evidence resulted in clinically significant reclassification of 38 (84.4%) variants, including three reclassified as pathogenic or likely pathogenic and 35 as likely benign. A total of 16 downgraded variants were independently downgraded by Invitae. These findings demonstrate that tumor mutational signatures can be formally incorporated into Bayesian germline interpretation, transforming tumor data into quantitative pathogenicity evidence and offering a principled strategy to reduce VUS burden in hereditary cancer genetics.

PMID 42719515
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PubMedFamilial cancer2026-09-10

Uptake of germline testing for Lynch Syndrome in patients with deficient mismatch repair/ microsatellite-high colorectal cancer in the public hospital system in South Australia.

Vembar Preethi P, Dow Eryn E

Lynch syndrome (LS) accounts for approximately 4% of colorectal cancer (CRC) cases and arises from pathogenic variants in mismatch repair (MMR) genes. Australian guidelines recommend universal MMR or microsatellite instability (MSI) screening in all CRC patients; however, real-world uptake remains variable. This study evaluated rates of MMR/MSI screening, germline testing, and genetics referrals across two major public hospitals in South Australia. A retrospective review of 1775 patients discussed at colorectal multidisciplinary team meetings in the Royal Adelaide and Queen Elizabeth hospitals between January 2021 and December 2023 was conducted to identify rates of MMR/MSI screening and subsequent referral of eligible patients to genetics. Of the 1129 colorectal cancer cases identified, MMR/MSI testing was performed in 93.2% (1052/1129), with deficiency detected in 12.5% (131/1052). Of these, 37% (49/131) were eligible for genetics referral after exclusion of somatic causes. Among eligible patients, 73.5% (36/49) were referred, and 43% (21/49) underwent germline testing. LS was confirmed in 12 patients (9% of deficient MMR CRC), while 9 patients (6.9%) were classified as having Lynch-like syndrome. Despite high screening rates, gaps remain in genetics referral and testing. Barriers included lack of reflex testing, loss to follow-up, and patient refusal. Targeted system-level interventions and improved genomic education are needed to enhance adherence to guidelines and optimise patient outcomes.

PMID 42720705
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PubMedJournal of the Pediatric Infectious Diseases Society2026-09-10

When Vaccination Meets Infection Prevention: National Practices for Inpatient Administration of Measles-Mumps-Rubella, Varicella, and Rotavirus Vaccines.

Altez Maria Susana Rueda MSR, Hutto Celia C, Hobby-Noland Delphene D, Song Xiaoyan X

PMID 42720270
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PubMedCureus2026-09-10

Zosteriform Cutaneous Metastasis of Lung Adenocarcinoma Mimicking Herpes Zoster: A Diagnostic Pitfall.

Gazal Ela E, Türsen Ümit Ü, Yuyucu Karabulut Yasemin Y

Zosteriform cutaneous metastasis from lung cancer is rare, but dermatomal distribution can lead to diagnostic anchoring on herpes zoster. A 65-year-old man with metastatic lung adenocarcinoma presented with a one-month history of painless, nonvesicular papules confined to the left T7-T9 dermatomes. Herpes zoster was initially suspected because of the striking unilateral dermatomal distribution and the patient's oncologic treatment-related immunosuppression, despite the absence of pain, vesiculation, and crusting. Oral valacyclovir was prescribed. The patient did not attend the planned one-week follow-up and next presented approximately six months later, when the eruption had progressed to extensive infiltrated violaceous papules and plaques spanning T2-T10. Histopathologic examination showed dermal infiltration by malignant gland-forming epithelial cells with lymphovascular invasion, and nuclear thyroid transcription factor-1 positivity supported pulmonary origin. The patient died approximately seven months following the diagnosis of cutaneous metastasis. This case documents the progression of initially limited zosteriform lesions to extensive infiltrative cutaneous metastases. In patients with malignancy, dermatomal distribution should not outweigh discordant morphology or clinical behavior; painless, nonvesicular, persistent, or progressive eruptions warrant early biopsy.

PMID 42719039
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