新冠病毒抗體檢測

確定您是否己被新冠病毒感染,或對新冠病毒產生了免疫反應

Semi-quantitative SARS-CoV-2 (COVID-19) IgG Antibody Serology Test

Confirm Immune Response to SARS-CoV-2


高度準確

靈敏度 (Sensitivity): 99.9%

特異性(Specificity): 99.9%

確認自己是否曾受感染,或對新冠肺炎病毒產生了免疫反應

  • 本抗體檢測針對血液中的新冠肺炎抗體(SARS-CoV-2/COVID-19 IgG antibodies)

  • 陽性檢測結果意味著人體已對SARS-CoV-2新冠病毒產生了免疫反應

  • 抗體是人體應對感染所產生的蛋白質。即使在感染期間沒有症狀,也可以產生抗體。

    檢測效益

  • 確認自己對新冠病毒己產生了免疫反應

  • 有抗體的您,己產生了免疫反應,不需要花費時間和金錢重複新冠肺炎病毒核酸檢測

  • 大多數醫學專家認為,抗體可以讓患者對新冠肺炎 (COVID-19)得到短期的免疫能力 (1-3)。但我們不知道這種免疫力能持續多久

  • 本檢測高度準確,特異性為99.9%,大大減少假陽性報告(假陽性意思是您沒有抗體,但檢測錯誤地報告您有抗體)

  • 由於人體對這種病毒的免疫反應尚不清楚,檢測結果不能用於確定免疫水平

  • 檢測申請經由Rainbow醫學總監批准。檢測結果絕對保密。

    誰應該考慮接受此測試

  • 前線醫護人員,公共汽車/出租車司機,零售人員,警察以及經常與公眾接觸的人,長者,及想知道自己是否已經有新冠病毒抗體的人。


  • 患者可以到我們的合作診所抽血

  • 樣品送到全球最大的診斷實驗室之一,Quest Diagnostics 完成測試

  • 檢測時間約為14到18天。

  • 提供 Quest Diagnostics 英文原文檢測報告,和中文檢測結果解釋


  • 本抗體檢測不是一項病毒檢測

  • 如果您現在有新冠肺炎症狀,請立即進行病毒核酸檢測以確認您當前的感染情況


關於此抗體檢測的信息和免責聲明

  • 檢測靈敏度為> 99.9% (症狀發作後至少15天收集的樣本的估計) (5)

  • 通過NPA4的交叉反應研究評估,估計的檢測特異性約為99.9%(5)

  • 檢測結果以報告指數 ≥1.00為陽性(5)。這個陽性的結果意味著一個人已經對SARS-CoV-2病毒產生了免疫反應。

  • 由於對這種病毒的人體免疫反應尚不清楚,因此檢測結果不能用於指示免疫水平或排除再次感染的機會(5)。

  • 報告指數5小於1.00為陰性,這意味著患者血清樣本中沒有SARS-CoV-2病毒IgG抗體,或者患者樣本中抗體的相對水平低於指數臨界值(5, 7)。

  • 注意:報告指數不應用於量度對SARS-CoV-2感染或再感染的免疫力的持久性。對SARS-CoV-2的免疫力的持久性和持續時間仍未明確定義,並且仍然是全世界科學與公共衛生研究的領域(8)。

  • 本SARSCoV-2 IgG檢測不應用來診斷急性SARS-CoV-2感染。

  • 本SARSCoV-2 IgG檢測僅限於經過1988年臨床實驗室改進修正案 CLIA,42 U.S.C 263a 認證的實驗室,以進行中度或高度複雜性檢測。


Quest Diagnostics

SARS-CoV-2 Serology (COVID-19) Antibody (IgG), Immunoassay

  • Presence of IgG antibodies may indicate an immune response to SARS-CoV-2.

  • A positive result may suggest an immune response to a primary infection with SARS-CoV-2, but the relationship between IgG positivity and immunity to SARS-CoV-2 has not yet been firmly established.

  • Antibody tests should not be used to definitively diagnose or exclude SARS-CoV-2 infection.

  • Positive results could also be due to past or present infection with non-SARS-CoV-2 coronavirus strains, such as coronavirus HKU1, NL63, OC43, or 229E.

  • Diagnosis of COVID-19 is made by detection of SARS-CoV-2 RNA by molecular testing methods, consistent with a patient's clinical findings.

  • SARS-CoV-2 IgG antibody assays offered by Quest Diagnostics have been authorized through the U.S. FDA EUA (Emergency Use Authorization) process.


  • Sensitivity: 99.9%

  • Specificity: 99.9%


Test Information and Disclaimer

  • Estimated assay sensitivity is >99.9% for specimens collected at least 15 days post-symptom onset(5)

  • Estimated assay specificity is approximately 99.9% based on NPA4 assessed by performing cross-reactivity studies(5)

  • Test result is reported as positive at an index of ≥1.00 (5). This positive result means that an individual has developed an immune response to SARS-CoV-2.

  • Since much is still not known about the body’s immune response to this virus, this test result cannot be used to indicate a level of immunity or rule out the chance for reinfection. (5)

  • Negative result is reported at an index of <1.00 (5), which means that the patient serum specimen had no SARS-CoV-2 spike IgG antibodies, or that the relative level of antibodies in the patient specimen was below the index cutoff.(5, 7)

  • Note: this index value should not be interpreted as a measurement of durable immunity or protection from SARS-CoV-2 infection or reinfection. Durability and duration of immunity to SARS-CoV-2 is still not clearly defined and continues to be an area of national and global scientific and public health research.(8)

  • The SARSCoV-2 IgG assay should not be used to diagnose acute SARS-CoV-2 infection.

  • Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) of 1988, 42 U.S.C 263a, to perform moderate or high complexity test.


Purchase the Antibody Test

購買抗體檢測

HK$2300

  • 請電話 或 Whatsapp 聯繫 9144 9238,安排訂購抗體檢測。

  • Call or Message (Whatsapp) 9144 9238, arrange to order a test.

  • 請前往我們的其中一個診所/實驗室提供血液樣本。Go to one of our clinics/labs to provide a blood sample.

  • 檢測報告將在14到18天之內使用安全的交付方案提供給您。Test report will be provided to you using secured delivery protocols within 14-18 days.

  • 患者直接付款價格為 HK$2300.(包括所有運輸費用和血液樣本出口文件費用)。We offer a patient-pay price of HK$2300 per test (All shipping cost and blood sample export documentation cost included).

  • 家庭檢測或多個檢測可享受額外折扣。Additional discounts available for family testing or multiple test orders.

  • 樣本收集診所/實驗室地點 - 中環,砲台山,銅鑼灣,旺角及尖沙咀。
  • Sample Collection Clinic/Lab Locations - Central, Fortress Hill, Causeway Bay, Mongkok & Tsi Sha Tsui.

  • 檢測申請經由Rainbow醫學總監批准,結果絕對保密. All antibody test requisitions are reviewed and approved by Rainbow’s medical director. Patient and data privacy is confidentially-protected.


Samples are sent to Quest Diagnostics, one of the world’s largest diagnostic service providers


Additional Antibody Tests Available

  1. Rabies

  2. Bordetella pertussis

  3. Diphtheria

  4. Tetanus

  5. Polio virus

  6. Hepatitis B

  7. Streptococcus pneumoniae

  8. Measles

  9. Mumps

  10. Rubella

  11. Chicken pox

  12. Haemophilus influenzae B


其他抗體測試

送往

Quest Diagnostics

進行檢測

  1. 狂犬病/疯狗 

  2. 百日咳

  3. 白喉

  4. 破傷風

  5. 脊髓灰質炎病毒

  6. 乙型肝炎

  7. 肺炎鏈球菌

  8. 麻疹

  9. 腮腺炎

  10. 麻疹

  11. 水痘

  12. 乙型流感


Test Procedure

  • Samples are immediately sent to Quest Diagnostics via FedEx

  • English test reports and a Chinese interpretation guide are provided to ordering physicians and patients

  • Turnaround time is about 14-18 days

  • 樣品會立即通過FedEx發送到Quest Diagnostics

  • 檢測時間約為14到18天

  • 提供 Quest Diagnostics 英文原文檢測報告,和中文檢測結果解釋



Reference/ 醫學文獻

  1. Humoral Immune Response to SARS-CoV-2 in Iceland. New England Journal of Medicine. 2020 Sep 1. doi: 10.1056/ NEJMoa2026116.

  2. Detection, prevalence, and duration of humoral responses to SARS2 CoV-2 under conditions of limited population exposure. https://doi.org/10.1101/2020.08.14.20174490. Prepirnt version posted August 16, 2020.

  3. Functional SARS-CoV-2-specific immune memory persists after mild COVID-19. https://doi.org/10.1101/2020.08.11.20171843. Preprint version posted August 15, 2020.

  4. Coronavirus Disease 2019 (COVID-19) - Test for Past Infection. https://www.cdc.gov /coronavirus/2019-ncov/testing/serology-overview. Updated June 30, 2020. Centers for Disease Control and Prevention

  5. Atellica® IM SARS-CoV-2 IgG (COV2G) and ADVIA® Centaur SARS-CoV-2 IgG (COV2G). Instructions for use. Siemens Healthcare Diagnostics Inc; 2020. Accessed February 14, 2021.

  6. EUA authorized serology test performance. US Food and Drug Administration. Updated October 14, 2020. Accessed January 21, 2021.

  7. Fact sheet for healthcare providers: Siemens Healthcare Diagnostics Inc. Atellica® IM SARS-CoV-2 IgG (COV2G). SARS-CoV-2 IgG semi-quantitative and ADVIA Centaur® SARS-CoV-2 IgG (COV2G). US Food and Drug Administration.

  8. Reinfection with COVID-19. Centers for Disease Control and Prevention. Updated October 27, 2020. Accessed January 22, 2021.