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Abstrak :
ABSTRAK
Tungau debu rumah merupakan sumber alergen yang dapat menyebabkan alergi. Menurut biofisika, terjadinya alergi dalam tubuh manusia adalah hasil munculnya pencetakan alergi allergy imprinting yang berasal dari kontak tubuh manusia dengan zat dan berkembang dari pencetakan biofisik dengan substansi informasi. Penelitian dirancang dengan desain eksperimental untuk menilai dampak bioresonansi gelombang elektromagnetik terhadap perubahan profil mediator pro inflamasi type 2 IL4 dan IL13 dan mediator anti inflamasi IL10 yang dihasilkan oleh kultur sel darah lengkap yang diambil dari subjek alergi rhinitis karena tungau debu rumah. Hasil menunjukkan bahwa pada group dengan perlakuan bioresonansi didapatkan perbedaan. IL 4 dan IL13 yang diberi antigen tungau terhadap kontrol negatif lebih rendah dibandingkan dengan group yang tanpa perlakuan bioresonansi. Kadar IL10 sebagai mediator anti inflamasi lebih meningkat dibandingkan dengan group tanpa perlakuan bioresonansi. Hasil analisa respon sel darah lengkap yang menunjukkan kenaikan dari kondisi kontrol RPMI dibandingkan terhadap PHA Phytohemagglutinin menggambarkan bahwa kelompok dengan perlakuan bioresonansi dan yang tidak diberi perlakuan bioresonansi pada hari ke-7 masih hidup dan menghasilkan produksi sitokin. Produksi meditor akibat perlakuan bioresonansi gelombang elektromagnetik tidak mengubah fungsi biologik dari peran anti inflamasi yang secara fungsional dapat menghambat laju produksi inflamasi. Kata kunci: alergi tungau debu rumah, bioresonansi, interleukin

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ABSTRACT
House dust mites are a source of allergens that can cause allergies. In the view of biophysics the occurrence of allergies in the human body is the result of the emergence of allergy imprinting which comes from human body contact with substances and evolves from biophysical printing with the substance of information. The study was designed with an experimental design to assess the impact of bioresonance of electromagnetic waves on changes in pro inflammatory mediator profiles IL 4 and IL 13 and anti inflammatory mediators IL 10 produced by complete blood cell cultures drawn from subjects of rhinitis allergy due to dust mites home. The result shows that the group given the bioresonance treatment, the difference between IL 4 and IL 13 given the mite antigen to negative control is lower than that of group without treatment. Level of IL 10 as an anti inflammatory mediator is increased compared to the group without bioresonance treatment. Result of a complete blood cell response analysis which shows an increase in control condition RPMI compared to PHA Phytohemagglutinin illustrates that the exposed group and non exposed to bioresonance on the 7th day are viable and produce cytokine production. The production of meditators due to the exposure of programmed bioresonance treatment does not alter the biological functioning of the anti inflammatory role that functionally is able to inhibit the rate of inflammatory production.

Abstrak :
ABSTRAK
Latar Belakang: Atopi yang ditandai dengan sensitisasi (produksi IgE) terhadap alergen merupakan faktor risiko untuk terjadinya penyakit alergi. Karena komposisi genetik cenderung stabil, peningkatan prevalensi penyakit alergi diduga disebabkan oleh faktor lingkungan yang berubah.

Tujuan: Mengetahui faktor yang memengaruhi sensitisasi terhadap alergen hirup dan munculnya manifestasi penyakit alergi pada populasi dewasa muda di Indonesia.

Metode: Penelitian potong lintang dilakukan pada mahasiswa baru Universitas Indonesia tahun 2019. Mahasiswa diminta mengisi kuesioner berisi data demografi, kuesioner International Study of Asthma and Allergies in Childhood (ISAAC), menjalani pemeriksaan fisik dan uji cukil kulit terhadap lima alergen hirup (kecoa, Dermatophagoides farinae, Dermatophagoides pteronyssinus, bulu kucing, epitel anjing). Sensitisasi ditandai dengan terdapat setidaknya satu hasil positif pada uji cukil kulit. Jika terdapat hasil positif pada dua atau lebih alergen, subyek disebut mengalami polisensitisasi. Manifestasi alergi yang dinilai berupa asma, rinitis alergi, dan dermatitis atopi.

Hasil: Proporsi sensitisasi adalah 44,8% (128 dari 286 subyek), sedangkan proporsi manifestasi penyakit alergi adalah 57,7% (165 dari 258 subyek). Manifestasi penyakit alergi didapatkan pada 84 (65,6%) subyek dari subkelompok yang tersensitisasi. Sensitisasi ditemukan lebih banyak pada laki-laki (OR 2,25; IK95% 1,38-3,71; p=0,001) dan subyek yang lahir secara caesar (OR 2,46; IK95% 1,22-5,06; p=0,013), sebaliknya lebih sedikit pada subyek yang berasal dari urban (OR 0,54; IK95% 0,32-0,90; p=0,019). Subyek yang tersensitisasi cenderung untuk memiliki manifestasi penyakit alergi (OR 1,79; IK95% 1,10-2,95; p=0,020). Pada subkelompok yang tersensitisasi, manifestasi penyakit alergi ditemukan lebih banyak pada subyek yang tinggal di urban (OR 2,58; IK95% 1,15-6,01; p=0,024), obese (OR 5,25; IK95% 1,35-34,92; p=0,036), dan mengalami polisensitisasi (OR 2,26; IK95% 1,01-5,10; p=0,046).

Simpulan: Sensitisasi terhadap alergen hirup dipengaruhi oleh jenis kelamin lakilaki, status urban, dan riwayat persalinan caesar. Munculnya manifestasi penyakit alergi dipengaruhi oleh adanya sensitisasi. Pada subkelompok yang tersensitisasi, munculnya manifestasi penyakit alergi dipengaruhi oleh status urban, obesitas, dan polisensitisasi.

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ABSTRACT
Background: Atopy marked by allergen sensitization (IgE production) is a risk factor for allergic diseases. Since genetic composition tends to be stable, the increase of allergic diseases prevalence is suspected due to changing environment factors.

Purpose: To identify the factors affecting sensitization to inhalant allergen and allergic diseases manifestation in Indonesian young adults.

Methods: Cross-sectional study done on Universitas Indonesia 2019 new students. Students were asked to fill in a demographic questionnaire, an International Study of Asthma and Allergies in Childhood (ISAAC) questionnaire, undergo physical examination and skin prick tests for five inhalant allergens (cockroach, Dermatophagoides farinae, Dermatophagoides pteronyssinus, cat hair, dog epithelium). Sensitization was marked by at least one positive result on the skin prick test. If there were two or more positive allergen results, subject was deemed as being polysensitized. Evaluated allergic manifestations were asthma, allergic rhinitis, dan atopic dermatitis.

Result: Sensitization was found in 44.8% (128 out of 286 subjects), while allergic diseases clinical manifestation was found in 57.7% (165 out of 258 subjects). The manifestation was found in 84 (65.6%) subjects from the sensitized subgroup. Sensitization was found more on male (OR 2.25; 95%CI 1.38-3.71; p=0.001) and subjects born by caesarean section (OR 2.46; 95%CI 1.22-5.06; p=0.013), whereas fewer on subjects from urban (OR 0.54; 95%CI 0.32-0.90; p=0.019). Sensitized subjects tended to demonstrate allergic diseases manifestation (OR 1.79; 95%CI 1.10-2.95; p=0.020). In the sensitized subgroup, allergic diseases manifestation was found more on subjects living in urban (OR 2.58; 95%CI 1.15-6.01; p=0.024), are obese (OR 5.25; 95%CI 1.35-34.92; p=0.036), and are polysensitized (OR 2.26; 95%CI 1.01-5.10; p=0.046).

Conclusion: Sensitization to inhalant allergens was affected by male sex, urbanstatus, and caesarean section birth. Allergic diseases manifestation was affected by presence of sensitization. In the sensitized subgroup, allergic diseases manifestation was affected by urban status, obesity, and polysensitization.

Abstrak :
Latar belakang: Saat ini prevalens alergi semakin meningkat. Terapi alergi lebih terfokus untuk mengatasi gejala simptomatik. Pendekatan lain adalah terapi imunomodulasi dengan agonis toll like receptor (TLR) 9 yang dapat mengalihkan respon imun sel TCD4+ Th2 ke arah Th1. CpG ODN 2006x3_PD adalah oligonukleotida sintetik kelas B merupakan agonis TLR9 yang berpotensi aman karena mengandung fosfodiester. Pada penelitian ini CpG ODN 2006x3_PD diuji kemampuan untuk mengatasi alergi dengan menggunakan penghantar nanopartikel kitosan, melalui uji in vitro pada sel mononukleus darah tepi dan in vivo pada hewan coba mencit alergi. Metode: Preparasi nanopartikel kitosan dilakukan dengan metode gelasi ion, melalui reaksi ikat silang kitosan dan tripolifosfat. Nanopartikel dikarakterisasi dengan Dynamic light scattering (DLS), zeta sizer dan transmission electron microscope (TEM). Uji pengikatan dilakukan dengan elektroforesis pada gel agarosa 12%, uji toksisitas dan kemampuan aktivasi NF-κB dilakukan pada sel RAW Blue, dengan menggunakan cel counting kit 8 dan kit Quanti blue. Sel mononukleus darah tepi yang distimulasi selama 7 hari pada uji in vitro dan plasma hewan coba mencit Balb/c pada uji in vivo diukur konsentrasi IFNγ, IL-10, IL-13 dan IgE dengan metode ELISA. Hasil: Diperoleh nanopartikel dengan ukuran <300 nm, muatan permukaan positif, bentuk sferis, tidak toksik dan dapat mengaktivasi NF-κB. Uji in vitro pada sel mononukleus darah tepi menunjukkan CpG ODN 2006x3_PD yang dihantarkan nanopartikel kitosan dapat menstimulasi sitokin tipe Th1 IFNγ dan T reg IL-10, menurunkan sitokin tipe Th2 IL-13 namun belum dapat menurunkan secara bermakna produksi IgE total pada sel mononukleus darah tepi individu sehat dan alergi Aplikasi intra nasal 10 ug/kali, 3 kali seminggu selama 3 minggu CpG ODN 2006x3_PD dan CpG ODN 2006x3_PD yang dihantarkan nanopartikel kitosan pada mencit Balb/c yang diinduksi alergi dengan ovalbumin dapat menstimulasi sitokin tipe Th1 IFNγ dan Treg IL-10, namun belum dapat menurunkan secara bermakna sitokin tipe Th2 IL-13 pada plasma mencit. Aplikasi CpG ODN 2006x3_PD dapat menurunkan produksi IgE spesifik anti ovalbumin pada plasma mencit meskipun belum dapat menurunkan produksi IgE total. Simpulan: CpG ODN 2006x_PD dapat menjadi kandidat imunostimulator yang potensial pada alergi.

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Background: Currently, prevalence of allergy has increased in worldwide. Allergy treatment is mainly focused to reduce clinical symptoms. Another approach is immunomodulation therapy which utilizes toll like receptor (TLR) 9 agonist that may redirect pro-allergenic Th2 biased CD4+ T cell response toward Th1. CpG ODN 2006x3_PD which is classified as synthetic oligonucleotides B has potential as a safe TLR9 agonist due to its natural backbone. In this study, CpG ODN 2006x3_PD was examined about its ability in overcoming allergies by using chitosan nanoparticles delivery, through in vitro tests on peripheral blood mononuclear cells and in vivo through allergic mice animal model. Methods: Chitosan nanoparticles was prepared by ionic gelation method, through crosslinking reaction of chitosan and tripolyphosphate. Nanoparticles are characterized by Dynamic light scattering (DLS), zeta sizer and transmission electron microscope (TEM). The binding test was carried out with electrophoresis on 12% agarose gel, toxicity test and NF-κB activation ability performed on RAW Blue cells, using cel counting kit 8 and Quanti blue kit. IFNγ, IL-10, IL-13 and IgE level of in vitro tests of peripheral blood mononuclear cells after 7 days stimulation and Balb/c mice plasma of in vivo study were measured by ELISA method. Results: Less than 300 nm, positive surface charge, spherical shape and nontoxic chitosan nanoparticles were obtained. These nanoparticles could deliver CpG ODN to activate NF-κB of mouse RAW-Blue cells effectively. In vitro assays of peripheral blood mononuclear cells showed that CpG ODN 2006x3_PD delivered by chitosan nanoparticles may stimulate Th1 IFNγ and T reg type cytokines IL-10, also decrease the Th2-type cytokine IL-13 but it couldn't inhibit total IgE production in peripheral blood mononuclear cells significantly. Intranasal application of 10 ug, 3 times per week for 3 weeks of CpG ODN 2006x3_PD and CpG ODN 2006x3_PD which were delivered by chitosan nanoparticles in allergen induced Balb/c mice could stimulate Th1 IFNγ and Treg type cytokines IL-10, but it couldn't significantly reduce the Th2-type cytokine IL-13 in mice plasma . The CpG ODN application decreased the specific IgE production of anti ovalbumin in mice plasma although it couldn't significantly reduce total IgE production. Conclusions: CpG ODN 2006x_PD could be a potential candidate for allergic immunostimulator.