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Evidence for New Standard of Care in Non-Small Cell Lung Cancer Patients

Despite many recent advances in treatment, the prognosis of lung cancer patients remains poor, with 5-year survival rates ≤15%. The treatment of nonsmall cell lung cancer (NSCLC) can include surgery, radiation, and chemotherapy, depending on the stage at the time of diagnosis.
These treatments as well as the disease itself can be extremely burdensome. In a systematic review of the literature, lung cancer patients were found to report on average 14 symptoms throughout the trajectory of illness. Newly diagnosed patients most commonly reported fatigue, dyspnea, pain, and cough, in addition to anxiety and depression. Similarly, the incidence of chronic postthoracotomy pain in patients with early-stage lung cancer ranges from 26% to 67%.
Although the prevalence of postthoracotomy pain decreas...

The Impact of Vitamin D on Regulatory T Cells

 

Epidemiologic studies highlight the increasing prevalence of vitamin D deficiency and insufficiency and its association with an increased risk of autoimmune diseases and poor respiratory function, including asthma.

These and additional studies have raised interest in the immunomodulatory properties of vitamin D beyond its well-established role in calcium homeostasis and bone health. Vitamin D has been shown to influence the function of cells intrinsic to innate and adaptive immunity.

This review discusses recent evidence that vitamin D promotes—both directly and indirectly—regulatory or suppressor T-cell populations with the capacity to inhibit inappropriate immune responses that cause disease, suggesting that this property may in part underpin the epidemiologic findings.

New Developments in the Use of Histamine and Histamine Receptors

 

Histamine and the histamine receptors are important regulators of a plethora of biological processes, including immediate hypersensitivity reactions and acid secretion in the stomach.

In these roles, antihistamines have found widespread therapeutic applications, while the last receptor to be discovered, the H4 histamine receptor, has become a major target of novel therapeutics. Recent studies involving human genetic variance and the development of mice lacking specific receptors or the ability to generate histamine have shown roles for the histamine pathway that extend well beyond the established roles. These include identification of previously unappreciated mechanisms through which histamine regulates inflammation in allergy, as well as roles in autoimmunity, infection, and pain.

As a result, antihistamines may have wider applications in the future than previously predicted.

How Should Allergists Deal With Local Reactions to Allergen Immunotherapy?

 

Despite the well-known benefits of subcutaneous immunotherapy (SCIT), adverse reactions include both local reactions (LRs) and systemic reactions.

An LR is a well-known adverse event associated with SCIT injections and is defined as any swelling located at or near the injection site following allergen injection. Concerns that LRs might predict systemic reactions have historically motivated allergists to dose adjust for LRs.

More recent data have dispelled this notion, although many allergists continue to dose adjust for other reasons. This article discusses the historical response to LRs and dose adjustments and reviews the most recent literature addressing LRs to SCIT.

Treatment options, although they are either unproven or not studied, are offered as an alternative to routine dose adjustments for LRs. Education remains the foundation of physician–patient communication concerning LRs.

The Role of Complement in the Diagnosis and Management of Allergic Rhinitis and Allergic Asthma

Allergic rhinitis and asthma are common chronic inflammatory diseases of the nasal mucus membranes and the upper airways with a high prevalence in Western countries. In addition to maladaptive T-helper type 2 (Th2) immunity, Th17 cells can drive the inflammatory responses in both diseases.

Several reports have shown that the complement system is activated locally and systemically in allergic rhinitis and/or allergic asthma patients. Importantly, recent findings in experimental models of allergic rhinitis and allergic asthma suggest that the complement cleavage products complement 3a and complement 5a and the activation of their corresponding receptors in antigen-presenting cells regulate the development of maladaptive Th2 and Th17 immunity. These findings in experimental asthma are corroborated by genome-wide searches and candidate gene studies in humans.

We discuss recent findings in experimental and human allergic airway diseases suggesting that complement may serve as a new diagnostic and therapeutic target for both disorders.

 

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